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1.

図書
図書
1. Trypanosomes : after the genome
edited by David Barry ... [et al.]
出版情報: Wymondham : Horizon Bioscience, c2007  xi, 423 p. ; 24 cm
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2.

図書
図書
2. Regio- and stereo-controlled oxidations and reductions
edited by Stanley M. Roberts, John Whittall
出版情報: Chichester : J. Wiley & Sons, c2007  xxii, 312 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 5
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Series Preface
Preface to Volume 5
Abbreviations
Industrial Catalysts for Regio- or Stereo-Selective Oxidations and Reductions A Review of Key Technologies and Targets / John Whittall1：
Introduction / 1.1：
Reduction of Carbon-Carbon Double Bonds / 1.2：
Privileged structures: [alpha]-amino acids and itaconic acids / 1.2.1：
[beta]-Amino acids / 1.2.2：
[alpha]-Alkyl substituted acids / 1.2.3：
[alpha]-Alkoxy substituted acids / 1.2.4：
Unsaturated nitriles / 1.2.5：
Alkenes and allyl alcohols / 1.2.6：
[alpha],[beta]-Unsaturated aldehyde reduction / 1.2.7：
Ketone and Imine Reduction / 1.3：
Catalytic hydrogenation of ketones and imines / 1.3.1：
Asymmetric transfer hydrogenation (ATH) catalysts / 1.3.2：
Modified borane reagents / 1.3.3：
Biocatalysts (alcohol dehydrogenases and ketoreductases) / 1.3.4：
Oxidation / 1.4：
Sharpless chiral epoxidation of allyl alcohols / 1.4.1：
Dioxirane catalyzed epoxidation / 1.4.2：
Amines and iminium salts / 1.4.3：
Phase transfer catalysts / 1.4.4：
The Julia-Colonna method (polyleucine oxidation) / 1.4.5：
Organocatalytic [alpha]-hydroxylation of ketones / 1.4.6：
Baeyer-Villiger oxidation / 1.4.7：
Chiral sulfoxides / 1.4.8：
References
Asymmetric Hydrogenation of Alkenes, Enones, Ene-Esters and Ene-Acids / 2：
(S)-2,2[prime]-Bis{[di(4-methoxyphenyl)phosphinyl]oxy}-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-octahydro-1,1[prime]-binaphthyl as a ligand for rhodium-catalyzed asymmetric hydrogenation / Ildiko Gergely ; Csaba Hegedus ; Jozsef Bakos2.1：
Synthesis of (S)-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-Octahydro-1,1[prime]-bi-2-naphthol / 2.1.1：
Synthesis of (S)-2,2[prime]-Bis{[di(4-methoxyphenyl)phosphinyl]oxy}-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-octahydro-1,1[prime]-binaphthyl / 2.1.2：
Asymmetric hydrogenation of Dimethyl itaconate / 2.1.3：
Conclusion
Synthesis and application of phosphinite oxazoline iridium complexes for the asymmetric hydrogenation of alkenes / Frederik Menges ; Andreas Pfaltz2.2：
Synthesis of (4S,5S)-2-(5-Methyl-2-phenyl-4,5-dihydro-oxazol-4-yl)-1,3-diphenyl-propan-2-ol / 2.2.1：
Synthesis of (4S,5S)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydro-oxazol-4-yl)-2-phenyl-ethyl]-diphenylphosphinite / 2.2.2：
Synthesis of (4S,5S)-[([eta superscript 4]-1,5-Cyclooctadiene)-{2-(2-phenyl-5-methyl-4,5-dihydro-oxazol-4-yl)-1,3-diphenyl-2-diphenylphosphinite-propane}iridium(I)]-tetrakis[3,5-bis(trifluoromethyl)phenyl]borate / 2.2.3：
Asymmetric hydrogenation of trans-[alpha]-Methylstilbene / 2.2.4：
Synthesis and application of heterocyclic phosphine oxazoline (HetPHOX) iridium complexes for the asymmetric hydrogenation of alkenes / Pier Giorgio Cozzi2.3：
Synthesis of (4S)-tert-Butyl-2-(thiophene-2-yl)-4,5-dihydrooxazole / 2.3.1：
Synthesis of (4S)-tert-Butyl-2-(3-diphenylphosphino-thiophene-2-yl)-4,5-dihydrooxazole / 2.3.2：
Synthesis of (4S)-[([eta superscript 4]-1,5-Cyclooctadiene)-{4-tert-butyl-2-(3-diphenylphosphino-thiophene-2-yl)-4,5-dihydrooxazole}iridium(I)]-tetrakis [3,5-bis(trifluoromethyl)phenyl]borate / 2.3.3：
(R)-2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphino]-3,3[prime]-bipyridine [(R)-Xyl-P-Phos] as a ligand for rhodium-catalyzed asymmetric hydrogenation of [alpha]-dehydroamino acids / Jing Wu ; Albert S.C. Chan2.3.4：
Synthesis of 3-Bromo-2,6-dimethoxypyridine / 2.4.1：
Synthesis of Bis(3,5-dimethylphenyl)phosphine chloride / 2.4.2：
Synthesis of 3-Bromo-2,6-dimethoxy-4-di(3,5-dimethylphenyl)phosphinopyridine / 2.4.3：
2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphinoyl]-3,3[prime]-bipyridine / 2.4.4：
Optical resolution of ([plus or minus])-6 with (-) or (+)-2,3-0,0[prime]-Dibenzoyltartaric acid monohydrate [(R)-6 or (S)-6)] / 2.4.6：
(R)-2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphino]-3,3[prime]-bipyridine [(R)-Xyl-P-Phos, (R)-1] / 2.4.7：
Preparation of the stock solution of [Rh(R-Xyl-P-Phos)(COD)]BF[subscript 4] / 2.4.8：
A typical procedure for the asymmetric hydrogenation of methyl (Z)-2-Acetamidocinnamate / 2.4.9：
(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline (QuinoXP) as a ligand for rhodium-catalyzed asymmetric hydrogenation of prochiral amino acid and amine derivatives / Tsuneo Imamoto ; Aya Koide2.5：
Synthesis of (R)-tert-Butyl(hydroxymethyl)methylphosphine-borane / 2.5.1：
Synthesis of (R)-Benzoyloxy(tert-butyl)methylphosphine-borane / 2.5.2：
Synthesis of (S)-tert-Butylmethylphosphine-borane / 2.5.3：
(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline (QuinoxP) / 2.5.4：
Asymmetric hydrogenation of Methyl (E)-3-acetylamino-2-butenoate catalyzed by Rh(I)-(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline / 2.5.5：
Rhodium-catalyzed asymmetric hydrogenation of indoles / Ryoichi Kuwano ; Masaya Sawamura2.6：
Synthesis of (R)-2-[(S)-1-(Dimethylamino)ethyl]-1-iodoferrocene / 2.6.1：
Synthesis of (R)-2-[(S)-1-(Diphenylphosphinyl)ethyl]-1-iodoferrocene / 2.6.2：
Synthesis of (R,R)-2,2[prime]-Bis[(S)-1-(diphenylphosphinyl)ethyl]-1,1[Prime]-biferrocene / 2.6.3：
Synthesis of (R,R)-2,2[Prime]-Bis[(S)-1-(diphenylphosphino)ethyl]-1,1[Prime]-biferrocene [abbreviated to (S,S)-(R,R)-PhTRAP] / 2.6.4：
Catalytic asymmetric hydrogenation of N-Acetyl-2-butylindole / 2.6.5：
Catalytic asymmetric hydrogenation of 3-Methyl-N-(p-toluenesulfonyl)indole / 2.6.6：
Asymmetric Reduction of Ketones / 3：
(R,R)-Bis(diphenylphosphino)-1,3-diphenylpropane as a versatile ligand for enantioselective hydrogenations / Natalia Dubrovina ; Armin Borner3.1：
Synthesis of (S,S)-1,3-Diphenylpropane-1,3-diol / 3.1.1：
Synthesis of (S,S)-Methanesulfonyloxy-1,3-diphenylpropane-1,3-diol / 3.1.2：
Synthesis of (R,R)-Bis(diphenylphosphino)-1,3-diphenylpropane / 3.1.3：
Synthesis of both enantiomers of 1-Phenylethanol by reduction of acetophenone with Geotrichum candidum IFO 5767 / Kaoru Nakamura ; Mikio Fujii ; Yoshiteru Ida3.2：
Cultivation of G. candidum IFO 5767 / 3.2.1：
Synthesis of (S)-1-Phenylethanol / 3.2.2：
Synthesis of (R)-1-Phenylethanol / 3.2.3：
Titanocene-catalyzed reduction of ketones in the presence of water. A convenient procedure for the synthesis of alcohols via free-radical chemistry / Antonio Rosales ; Juan M. Cuerva ; J. Enrique Oltra3.3：
Titanocene-catalyzed reduction of Acetophenone in the presence of water / 3.3.1：
Titanocene-catalyzed synthesis of Methyl 4-deuterio-4-phenyl-4-hydroxybutanoate / 3.3.2：
Xyl-tetraPHEMP: a highly efficient biaryl ligand in the [diphosphine RuCl[subscript 2] diamine]-catalyzed hydrogenation of simple aromatic ketones / Paul H. Moran ; Julian P. Henschke ; Antonio Zanotti-Gerosa ; Ian C. Lennon3.4：
Synthesis of Tri(3,5-dimethylphenyl)phosphine oxide / 3.4.1：
Synthesis of Bis(3,5-dimethylphenyl)-(2-iodo-3,5-dimethylphenyl)phosphine oxide / 3.4.2：
Synthesis of rac-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphinoyl]-biphenyl / 3.4.3：
Synthesis of rac-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl [abbreviated to (rac)-Xyl-tetraPHEMP] / 3.4.4：
Synthesis of [(R)-N,N-Dimethyl(1-methyl)benzylaminato-C[superscript 2],N]-{rac-4,4[prime],6,6[prime]-tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl}-palladium(II) tetrafluoroborate and separation of the diastereomers / 3.4.5：
Synthesis of (S)-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl: [abbreviated to (S)-Xyl-tetraPHEMP) and (R)-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl [abbreviated to (R)-Xyl-tetraPHEMP] / 3.4.6：
Synthesis of [(R)-Xyl-tetraPHEMP RuCl[subscript 2] (R,R)-DPEN] and [(S)-Xyl-tetraPHEMP RuCl[subscript 2] (S,S)-DPEN] / 3.4.7：
Reduction of Acetophenone using [(S)-Xyl-tetraPHEMP RuCl[subscript 2] (S,S)-DPEN] as a precatalyst / 3.4.8：
N-Arenesulfonyl- and N-Alkylsulfamoyl-1,2-diphenylethylenediamine ligands for ruthenium-catalyzed asymmetric transfer hydrogenation of activated ketones / Michel (Massoud S.) Stephan ; Barbara Mohar3.5：
Synthesis of N-Arenesulfonyl-1,2-diphenylethylenediamines / 3.5.1：
Preparation of Ru(II)-N-arenesulfonyl-1,2-diphenylethylenediamine complexes / 3.5.2：
Asymmetric transfer hydrogenation of Ethyl benzoylacetate / 3.5.3：
The synthesis and application of BrXuPHOS: a novel monodentate phosphorus ligand for the asymmetric hydrogenation of ketones / Martin Wills ; Yingjian Xu ; Garden Docherty ; Gary Woodward3.6：
Synthesis of (S)-BrXuPHOS / 3.6.1：
Synthesis of (S,S,SS)-BrXuPHOS-Ru-DPEN / 3.6.2：
General procedure of asymmetric hydrogenation of acetophenone / 3.6.3：
Acknowledgement
In Situ formation of ligand and catalyst: application in ruthenium-catalyzed enantioselective reduction of ketones / Jenny Wettergren ; Hans Adolfsson3.7：
Synthesis of (S)-3-Fluoro-1-phenylethanol / 3.7.1：
Synphos and Difluorphos as ligands for ruthenium-catalyzed hydrogenation of alkenes and ketones / Severine Jeulin ; Virginie Ratovelomanana-Vidal ; Jean-Pierre Genet3.8：
Synthesis of [RuCl((S)-SYNPHOS)(p-cymene)]Cl / 3.8.1：
Synthesis of [RuCl((S)-DIFLUORPHOS)(p-cymene)]Cl / 3.8.2：
Synthesis of [RuI((S)-DIFLUORPHOS)(p-cymene)]I / 3.8.3：
Synthesis of [NH[subscript 2]R[subscript 2]] [(RuCl(PP))[subscript 2]([Mu]-Cl)[subscript 3]] PP = SYNPHOS or DIFLUORPHOS and R = Me or Et / 3.8.4：
Synthesis of [NH[subscript 2]Me[subscript 2]][RuCl-(S)-DIFLUORPHOS][subscript 2][[Mu]-Cl][subscript 3] / 3.8.5：
Synthesis of in situ generated [RuBr[subscript 2]((S)-SYNPHOS)] and [RuBr[subscript 2]((S)-DIFLUORPHOS)] / 3.8.6：
An arene ruthenium complex with polymerizable side chains for the synthesis of immobilized catalysts / Estelle Burri ; Silke B. Wendicke ; Kay Severin3.9：
Synthesis of 2-Methyl-cyclohexa-2,5-dienecarboxylic acid 2-(2-methyl-acryloyloxy)-ethyl ester / 3.9.1：
Synthesis of [[eta superscript 6]-(2-Methyl-benzoic acid 2-(2-methyl-acryloyloxy)-ethyl ester)RuCl[subscript 2]][subscript 2] / 3.9.2：
Selective reduction of carbonyl group in [beta], [gamma]-unsaturated [alpha]-alpha-ketoesters by transfer hydrogenation with Ru-(p-cymene) (TsDPEN) / Minjie Guo ; Dao Li ; Yanhui Sun ; Zhaoguo Zhang3.10：
Synthesis of Di-[Mu]-chloro-bis[chloro([eta superscript 6]-1-isopropyl-4-methyl-benzene)ruthenium(II) / 3.10.1：
Synthesis of ([plus or minus])-Monotosylate-1,2-diphenyl-1,2-ethylenediamine / 3.10.2：
Synthesis of Ru complex Ru(p-cymene)(TsDPEN) / 3.10.3：
Ru-TsDPEN catalyzed transfer hydrogenation reaction of [beta],[gamma]-unsaturated-[alpha]-ketoesters / 3.10.4：
Preparation of polymer-supported Ru-TsDPEN catalysts and their use for the enantioselective synthesis of (S)-fluoxetine / Liting Chai ; Yangzhou Li ; Quanrui Wang3.11：
Synthesis of the supported ligand 9 / 3.11.1：
Synthesis of ligand 17 / 3.11.2：
General procedure for asymmetric transfer hydrogenation / 3.11.3：
Preparation of (S)-Fluoxetine hydrochloride / 3.11.4：
Polymer-supported chiral sulfonamide-catalyzed reduction of [beta]-keto nitriles: a practical synthesis of (R)-Fluoxetine / Guang-yin Wang ; Gang Zhao3.12：
Synthesis of (R)-3-Amino-1-phenyl-propan-1-ol / 3.12.1：
Synthesis of (R)-ethyl 3-hydroxy-3-phenylpropylcarbamate / 3.12.2：
Synthesis of (R)-3-(Methylamino)-1-phenylpropan-1-ol / 3.12.3：
Synthesis of (R)-Fluoxetine / 3.12.4：
Imine Reduction and Reductive Amination / 4：
Metal-free reduction of imines: enantioselective Bronsted acid-catalyzed transfer hydrogenation using chiral BINOL-phosphates as catalysts / Magnus Rueping ; Erli Sugiono ; Cengiz Azap ; Thomas Theissmann4.1：
Synthesis of (R)-2,2[prime]-Bis-methoxymethoxy-[1,1[prime]] binaphthalene (MOM-BINOL) / 4.1.1：
Synthesis of (R)-3,3[prime]-Diiodo-2,2[prime]-bis(methoxymethoxy)-1,1[prime]-binaphthalene / 4.1.2：
Synthesis of 3,3[prime]-Bis-(3,5[prime]-bis-trifluoromethyl-phenyl)-2,2[prime]-bismethoxymethoxy [1,1[prime]-binaphthalene] / 4.1.3：
Synthesis of (R)-3,3[prime]-[3,5-Bis(trifluoromethyl)phenyl]-1,1[prime]-binaphthylphosphate / 4.1.4：
General procedure for the transfer hydrogenation of ketimines / 4.1.5：
Synthesis of [1-(2,4-Dimethyl-phenyl)-ethyl]-(4-methoxy-phenyl)-amine / 4.1.6：
Metal-free Bronsted acid-catalyzed transfer hydrogenation: enantioselective synthesis of tetrahydroquinolines / Andrey P. Antonchick4.2：
General procedure for the transfer hydrogenation of quinolines / 4.2.1：
Synthesis of 7-Chloro-4-phenyl-1,2,3,4-tetrahydroquinoline / 4.2.2：
Synthesis of (S)-2-Phenyl-1,2,3,4-tetrahydroquinoline / 4.2.3：
Synthesis of (R)-2-(2-(Benzo[1,3]dioxol-5-yl)ethyl)-1,2.3,4-tetrahydro-quinoline / 4.2.4：
A highly stereoselective synthesis of 3[alpha]-Amino-23,24-bisnor-5[alpha]-cholane via reductive amination / Sharaf Nawaz Khan ; Nam Ju Cho ; Hong-Seok Kim4.3：
Synthesis of Tris[(2-ethylhexanoyl)oxy]borohydride / 4.3.1：
Synthesis of 3[alpha]-Acetamino-23,24-bisnor-5[alpha]-cholane / 4.3.2：
Synthesis of 3[alpha]-N-1-[N(3-[4-Aminobutyl])-1,3-diaminopropane]-23,24-bisnor-5[alpha]-cholane / 4.3.3：
Acknowledgements
Oxidation of Primary and Secondary Alcohols / 5：
Copper(Il) catalyzed oxidation of primary alcohols to aldehydes with atmospheric oxygen / Suribabu Jammi ; Tharmalingan Punniyamurthy5.1：
Synthesis of copper(II) complex 1 / 5.1.1：
Typical procedure for the oxidation of primary alcohols to aldehydes / 5.1.2：
Solvent-free dehydrogenation of secondary alcohols in the absence of hydrogen abstractors using Robinson's catalyst / G.B.W.L Ligthart ; R.H. Meijer ; J. v. Buijtenen ; J. Meuldijk ; J.A.J.M. Vekemans ; L.A. Hulshof5.2：
Dehydrogenation of 2-Octanol using Ru(OCOCF[subscript 3])[subscript 2](CO)(PPh[subscript 3])[subscript 2] as a catalyst / 5.2.1：
2-Iodoxybenzoic acid (IBX)/n-Bu[subscript 4]NBr/CH[subscript 2]Cl[subscript 2]-H[subscript 2]O: a mild system for the selective oxidation of secondary alcohols / Krisada Kittigowittana ; Manat Pohmakotr ; Vichai Reutrakul ; Chutima Kuhakarn5.3：
Synthesis of 1-Hydroxy-5-decanone / 5.3.1：
Hydroxylation, Epoxidation and Related Reactions / 6：
Proline-catalyzed [alpha]-aminoxylation of aldehydes and ketones / Yujiro Hayashi ; Mitsuru Shoji6.1：
Synthesis of (R)-2-Anilinoxypropanol / 6.1.1：
Synthesis of (R)-7-Anilinoxy-1,4-dioxaspiro[4.5]decan-8-one / 6.1.2：
Ru/Silia Cat TEMPO-mediated oxidation of alkenes to [alpha]-hydroxyacids / Rosaria Ciriminna ; Mario Pagliaro6.2：
Synthesis of Silia Cat TEMPO / 6.2.1：
Synthesis of 2-(4-Chlorophenyl)-1,2-propanediol / 6.2.2：
Synthesis of 2-(4-Chlorophenyl)-1,2-hydroxypropanoic acid / 6.2.3：
Catalytic enantioselective epoxidation of trans-disubstituted and trisubstituted alkenes with arabinose-derived ulose / Tony K. M. Shing ; Gulice Y.C. Leung ; To Luk6.3：
Synthesis of 2[prime],3[prime]-Diisobutyl acetal / 6.3.1：
Synthesis of ulose / 6.3.2：
Asymmetric epoxidation of trans-[alpha]-Methylstilbene using ulose as catalyst at 0 [degree]C / 6.3.3：
VO(acac)[subscript 2]/TBHP catalyzed epoxidation of 2-(2-Alkenyl)phenols. highly regio- and diastereoselective oxidative cyclisation to 2,3-Dihydrobenzofuranols and 3-Chromanols / Alessandra Lattanzi ; Arrigo Scettri6.4：
VO(acac)[subscript 2]/TBHP catalyzed epoxidation of 2-(3,7-Dimethyl-octa-2,6-dienyl)-phenol / 6.4.1：
VO(acac)[subscript 2]/TBHP/TFA catalyzed oxidative cyclization of 2-(3,7-Dimethyl-octa-2,6-dienyl)-phenol / 6.4.2：
An Oxalolidinone ketone catalyst for the asymmetric epoxidation of cis-olefins / David Goeddel ; Yian Shi6.5：
Amadori rearrangement to give 1-Dibenzylamino-1-deoxy-D-fructose / 6.5.1：
Acetal protection of 1-Dibenzylamino-1-deoxy-D-fructose / 6.5.2：
Hydrogenation of the Dibenzylamine / 6.5.3：
Phosgene cyclization of aminoalcohol / 6.5.4：
Alcohol oxidation / 6.5.5：
Synthesis of ketone 2 / 6.5.6：
Asymmetric epoxidation of cis-[beta]-Methylstyrene / 6.5.7：
[alpha]-Fluorotropinone immobilised on silica: a new stereoselective heterogeneous catalyst for epoxidation of alkenes with oxone / Giovanni Sartori ; Alan Armstrong ; Raimondo Maggi ; Alessandro Mazzacani ; Raffaella Sartorio ; France Bigi ; Belen Dominguez-Fernandez6.6：
Synthesis of silica KG-60-supported enantiomerically enriched [alpha]-Fluorotropinone / 6.6.1：
Synthesis of enantiomerically enriched epoxides / 6.6.2：
Asymmetric epoxidation catalyzed by novel azacrown ether-type chiral quaternary ammonium salts under phase-transfer catalytic conditions / Kazushige Hori ; Keita Tani ; Yasuo Tohda6.7：
Synthesis of precursor of the azacrown ether / 6.7.1：
Synthesis of the azacrown ether / 6.7.2：
Synthesis of the azacrown ether-type quaternary ammonium salt / 6.7.3：
Asymmetric epoxidation of (E)-Chalcone catalyzed by the azacrown ether-type quaternary ammonium salt as chiral PTC / 6.7.4：
Enantioselective epoxidation of olefins using phase transfer conditions and a chiral [azepinium][TRISPHAT] salt as catalyst / Jerome Vachon ; Celine Perollier ; Alexandre Martinez ; Jerome Lacour6.8：
Enantioselective epoxidation of 1-Phenyl-3,4-dihydronaphthalene / 6.8.1：
Catalytic asymmetric epoxidation of [alpha],[beta]-unsaturated esters promoted by a Yttrium-biphenyldiol complex / Masakatsu Shibasaki ; Hiroyuki Kakei ; Shigeki Matsunaga6.9：
Synthesis of (aS,R)-6,6[prime]-[(Propylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.1：
Synthesis of (aS,R)-2,2-[Oxybis(ethylene)dioxy]-6,6[prime]-[(propylene)dioxy]biphenyl / 6.9.2：
Synthesis of (S)-6,6[prime]-[Oxybis(ethylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.3：
Enantiomeric enrichment of (S)-6,6[prime]-[Oxybis(ethylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.4：
Catalytic asymmetric epoxidation of [alpha],[beta]-unsaturated esters / 6.9.5：
Catalytic enantioselective epoxidation of [alpha],[beta]-enones with a binol-zinc-complex / Ana Minatti ; Karl Heinz Dotz6.10：
Synthesis of (E)-(2S,3R)-Phenyl-(3-phenyloxiran-2-yl)methanone / 6.10.1：
Asymmetric epoxidation of Phenyl-2-(3[prime]-pyridylvinyl)sulfone using polyleucine hydrogen peroxide gel / Mike R. Pitts6.11：
Preparation of polyleucine-hydrogen peroxide gel / 6.11.1：
Synthesis of Phenyl-2-(3[prime]-pyridylvinyl) sulfone (2) / 6.11.2：
Oxidation of Ketones to Lactones or Enones / 7：
Synthesis of 2-(Phosphinophenyl)pyrindine ligand and its application to palladium-catalyzed asymmetric Baeyer-Villiger oxidation of prochiral cyclobutanones / Katsuji Ito ; Tsutomu Katsuki7.1：
Synthesis of (7R)-2-(2-Hydroxyphenyl)-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.1：
2-[2-(Diphenylphosphinoyl)phenyl]-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.2：
2-[2-(Diphenylphosphanyl)phenyl]-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.3：
Asymmetric Baeyer-Villiger oxidation of 3-Phenylcyclobutanone / 7.1.4：
(D)-Codeinone from (D)-Dihydrocodeinone via the use of modified o-iodoxybenzoic acid (IBX). A convenient oxidation of ketones to enones / Paul Mather7.2：
Synthesis of IBX / 7.2.1：
Synthesis of codeinone / 7.2.2：
Oxidative C-C Coupling / 8：
Enantioselective oxidative coupling of 2-Naphthols catalyzed by a novel chiral vanadium complex / Nan-Sheng Xie ; Quan-Zhong Liu ; Zhi-Bin Luo ; Liu-Zhu Gong ; Ai-Qiao Mi ; Yao-Zhong Jiang8.1：
Synthesis of 3,3-Diformyl-2,2[prime]-biphenol / 8.1.1：
Synthesis of chiral vanadium complexes / 8.1.2：
Catalytic oxidative coupling of 7-Alkoxy-1-naphthols by chiral vanadium complexes / 8.1.3：
Reference
Catalytic oxidative cross-coupling reaction of 2-Naphthol derivatives / Shigeki Habaue ; Tomohisa Temma8.2：
Synthesis of Methyl 2,2[prime]-dihydroxy-1,1[prime]-binaphthalene-3-carboxylate / 8.2.1：
Oxidative coupling of benzenes with [alpha],[beta]-unsaturated aldehydes by Pd(OAc)[subscript 2]/ HPMoV/ O[subscript 2] system / Tomoyuki Yamada ; Satoshi Sakaguchi ; Yasutaka Ishii8.3：
Synthesis of Cinnamaldehyde / 8.3.1：
Oxidation of Sulfides and Sulfoxides / 9：
The first example of direct oxidation of sulfides to sulfones by an osmate-molecular oxygen system / Boyapati M. Choudary ; Chinta Reddy ; V. Reddy ; Billakanti V. Prakash ; Mannepalli L. Kantam ; B. Sreedhar9.1：
Synthesis of osmate exchanged Mg-Al layered double hydroxides (LDH-OsO[subscript 4]) / 9.1.1：
Synthesis of Methyl phenyl sulfone or Methylsulfonylbenzene / 9.1.2：
Selective oxidation of sulfides to sulfoxides and sulfones using hydrogen peroxide in the presence of zirconium tetrachloride / Kiumar Bahrami9.2：
Oxidation of Benzyl 4-bromobenzyl sulfide to Benzyl 4-bromobenzyl sulfoxide using H[subscript 2]O[subscript 2] in the presence of zirconium tetrachloride / 9.2.1：
Oxidation of Benzyl 4-bromobenzyl sulfide to Benzyl 4-bromobenzyl sulfone using H[subscript 2]O[subscript 2] in the presence of zirconium tetrachloride / 9.2.2：
WO[subscript 3]-30 % H[subscript 2]O[subscript 2]-cinchona alkaloids: a new heterogeneous catalytic system for asymmetric oxidation and kinetic resolution of racemic sulfoxides / Vinay V. Thakur ; A. Sudalai9.3：
Synthesis of (R)-2-[[[3-Methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimadazole {(R)-(+)-Lansoprazole} / 9.3.1：
Synthesis of (R)-(+)-Phenyl benzyl sulfoxide / 9.3.2：
Benzyl-4,6-O-isopropylidene-[alpha]-(D)-glucopyranoside, 2-deoxy-2-[[(2-hydroxy-3,5-di-tert-butylphenyl)methylene]amino] as a ligand for vanadium-catalyzed asymmetric oxidation of sulfides / Raffaella Del Litto ; Guiseppina Roviello ; Francesco Ruffo9.4：
Synthesis of Benzyl-4,6-O-isopropylidene-[alpha]-D-glucopyranoside, 2-deoxy-2-[[(2-hydroxy-3,5-di-tert-butylphenyl)methylene]imine] / 9.4.1：
Oxidation of Thioanisole / 9.4.2：
Asymmetric sulfoxidation of aryl methyl sulfides with hydrogen peroxide in water / Alessando Scarso ; Giorgio Strukul9.5：
Synthesis of complex (R)-BINAP)PtCl[subscript 2] / 9.5.1：
Synthesis of complex [((R)-BINAP)Pt((OH)][subscript 2](BF[subscript 4])[subscript 2] / 9.5.2：
Stereoselective catalytic oxidation of aryl methyl sulfides / 9.5.3：
Index
Series Preface
Preface to Volume 5
Abbreviations
3.

図書
図書
3. Renaissance of sickle cell disease research in the genome era
Betty Pace
出版情報: London : Imperial College Press , Hackensack, N.J. : Distributed by World Scientific Pub., c2007  xxxv, 357 p. ; 27 cm
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4.

図書
図書
4. Mass spectrometry : principles and applications. 3rd ed (: hbk ; : pbk)
Edmond de Hoffmann, Vincent Stroobant
出版情報: Chichester, U.K. : J. Wiley, c2007  xii, 489 p. ; 26 cm
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目次情報: 続きを見る
Preface
Introduction
Principles
Diagram of a Mass Spectrometer
History
Ion Free Path
Ion Sources / 1：
Electron Ionization / 1.1：
Chemical Ionization / 1.2：
Proton transfer / 1.2.1：
Adduct formation / 1.2.2：
Charge-transfer chemical ionization / 1.2.3：
Reagent gas / 1.2.4：
Negative ion formation / 1.2.5：
Desorption chemical ionization / 1.2.6：
Field Ionization / 1.3：
Fast Atom Bombardment and Liquid Secondary Ion Mass Spectrometry / 1.4：
Field Desorption / 1.5：
Plasma Desorption / 1.6：
Laser Desorption / 1.7：
Matrix-Assisted Laser Desorption Ionization / 1.8：
Principle of MALDI / 1.8.1：
Practical considerations / 1.8.2：
Fragmentations / 1.8.3：
Atmospheric pressure matrix-assisted laser desorption ionization / 1.8.4：
Thermospray / 1.9：
Atmospheric Pressure Ionization / 1.10：
Electrospray / 1.11：
Multiply charged ions / 1.11.1：
Electrochemistry and electric field as origins of multiply charged ions / 1.11.2：
Sensitivity to concentration / 1.11.3：
Limitation of ion current from the source by the electrochemical process / 1.11.4：
Atmospheric Pressure Chemical Ionization / 1.11.5：
Atmospheric Pressure Photoionization / 1.13：
Atmospheric Pressure Secondary Ion Mass Spectrometry / 1.14：
Desorption electrospray ionization / 1.14.1：
Direct analysis in real time / 1.14.2：
Inorganic Ionization Sources / 1.15：
Thermal ionization source / 1.15.1：
Spark source / 1.15.2：
Glow discharge source / 1.15.3：
Inductively coupled plasma source / 1.15.4：
Gas-Phase Ion-Molecule Reactions / 1.15.5：
Formation and Fragmentation of Ions: Basic Rules / 1.17：
Electron ionization and photoionization under vacuum / 1.17.1：
Ionization at low pressure or at atmospheric pressure / 1.17.2：
Formation of aggregates or clusters / 1.17.3：
Reactions at the interface between source and analyser / 1.17.6：
Mass Analysers / 2：
Quadrupole Analysers / 2.1：
Description / 2.1.1：
Equations of motion / 2.1.2：
Ion guide and collision cell / 2.1.3：
Spectrometers with several quadrupoles in tandem / 2.1.4：
Ion Trap Analysers / 2.2：
The 3D ion trap / 2.2.1：
The 2D ion trap / 2.2.2：
The Electrostatic Trap or 'Orbitrap' / 2.3：
Time-of-Flight Analysers / 2.4：
Linear time-of-flight mass spectrometer / 2.4.1：
Delayed pulsed extraction / 2.4.2：
Reflectrons / 2.4.3：
Tandem mass spectrometry with time-of-flight analyser / 2.4.4：
Orthogonal acceleration time-of-flight instruments / 2.4.5：
Magnetic and Electromagnetic Analysers / 2.5：
Action of the magnetic field / 2.5.1：
Electrostatic field / 2.5.2：
Dispersion and resolution / 2.5.3：
Tandem mass spectrometry in electromagnetic analysers / 2.5.4：
Ion Cyclotron Resonance and Fourier Transform Mass Spectrometry / 2.6：
General principle / 2.6.1：
Ion cyclotron resonance / 2.6.2：
Fourier transform mass spectrometry / 2.6.3：
MS[superscript n] in ICR/FTMS instruments / 2.6.4：
Hybrid Instruments / 2.7：
Electromagnetic analysers coupled to quadrupoles or ion trap / 2.7.1：
Ion trap analyser combined with time-of-flight or ion cyclotron resonance / 2.7.2：
Hybrids including time-of-flight with orthogonal acceleration / 2.7.3：
Detectors and Computers / 3：
Detectors / 3.1：
Photographic plate / 3.1.1：
Faraday cup / 3.1.2：
Electron multipliers / 3.1.3：
Electro-optical ion detectors / 3.1.4：
Computers / 3.2：
Functions / 3.2.1：
Instrumentation / 3.2.2：
Data acquisition / 3.2.3：
Data conversion / 3.2.4：
Data reduction / 3.2.5：
Library search / 3.2.6：
Tandem Mass Spectrometry / 4：
Tandem Mass Spectrometry in Space or in Time / 4.1：
Tandem Mass Spectrometry Scan Modes / 4.2：
Collision-Activated Decomposition or Collision-Induced Dissociation / 4.3：
Collision energy conversion to internal energy / 4.3.1：
High-energy collision (keV) / 4.3.2：
Low-energy collision (between 1 and 100 eV) / 4.3.3：
Other Methods of Ion Activation / 4.4：
Reactions Studied in MS/MS / 4.5：
Tandem Mass Spectrometry Applications / 4.6：
Structure elucidation / 4.6.1：
Selective detection of target compound class / 4.6.2：
Ion-molecule reaction / 4.6.3：
The kinetic method / 4.6.4：
Mass Spectrometry/Chromatography Coupling / 5：
Elution Chromatography Coupling Techniques / 5.1：
Gas chromatography/mass spectrometry / 5.1.1：
Liquid chromatography/mass spectrometry / 5.1.2：
Capillary electrophoresis/mass spectrometry / 5.1.3：
Chromatography Data Acquisition Modes / 5.2：
Data Recording and Treatment / 5.3：
Data recording / 5.3.1：
Instrument control and treatment of results / 5.3.2：
Analytical Information / 6：
Mass Spectrometry Spectral Collections / 6.1：
High Resolution / 6.2：
Information at different resolving powers / 6.2.1：
Determination of the elemental composition / 6.2.2：
Isotopic Abundances / 6.3：
Low-mass Fragments and Lost Neutrals / 6.4：
Number of Rings or Unsaturations / 6.5：
Mass and Electron Parities, Closed-shell Ions and Open-shell Ions / 6.6：
Electron parity / 6.6.1：
Mass parity / 6.6.2：
Relationship between mass and electron parity / 6.6.3：
Quantitative Data / 6.7：
Specificity / 6.7.1：
Sensitivity and detection limit / 6.7.2：
External standard method / 6.7.3：
Sources of error / 6.7.4：
Internal standard method / 6.7.5：
Isotopic dilution method / 6.7.6：
Fragmentation Reactions / 7：
Electron Ionization and Fragmentation Rates / 7.1：
Quasi-Equilibrium and RRKM Theory / 7.2：
Ionization and Appearance Energies / 7.3：
Fragmentation Reactions of Positive Ions / 7.4：
Fragmentation of odd-electron cations or radical cations (OE[superscript [middle dot]+]) / 7.4.1：
Fragmentation of cations with an even number of electrons (EE[superscript +]) / 7.4.2：
Fragmentations obeying the parity rule / 7.4.3：
Fragmentations not obeying the parity rule / 7.4.4：
Fragmentation Reactions of Negative Ions / 7.5：
Fragmentation mechanisms of even electron anions (EE[superscript -]) / 7.5.1：
Fragmentation mechanisms of radical anions (OE[superscript [middle dot]-]) / 7.5.2：
Charge Remote Fragmentation / 7.6：
Spectrum Interpretation / 7.7：
Typical ions / 7.7.1：
Presence of the molecular ion / 7.7.2：
Typical neutrals / 7.7.3：
A few examples of the interpretation of mass spectra / 7.7.4：
Analysis of Biomolecules / 8：
Biomolecules and Mass Spectrometry / 8.1：
Proteins and Peptides / 8.2：
ESI and MALDI / 8.2.1：
Structure and sequence determination using fragmentation / 8.2.2：
Applications / 8.2.3：
Oligonucleotides / 8.3：
Mass spectra of oligonucleotides / 8.3.1：
Applications of mass spectrometry to oligonucleotides / 8.3.2：
Fragmentation of oligonucleotides / 8.3.3：
Characterization of modified oligonucleotides / 8.3.4：
Oligosaccharides / 8.4：
Mass spectra of oligosaccharides / 8.4.1：
Fragmentation of oligosaccharides / 8.4.2：
Degradation of oligosaccharides coupled with mass spectrometry / 8.4.3：
Lipids / 8.5：
Fatty acids / 8.5.1：
Acylglycerols / 8.5.2：
Bile acids / 8.5.3：
Metabolomics / 8.6：
Mass spectrometry in metabolomics / 8.6.1：
Exercises / 8.6.2：
Questions
Answers
Appendices
Nomenclature
Units
Definitions
Analysers
Detection
Ionization
Ion types
Fragmentation
Acronyms and abbreviations
Fundamental Physical Constants
Table of Isotopes in Ascending Mass Order / 4A：
Table of Isotopes in Alphabetical Order / 4B：
Isotopic Abundances (in %) for Various Elemental Compositions CHON
Gas-Phase Ion Thermochemical Data of Molecules
Gas-Phase Ion Thermochemical Data of Radicals
Literature on Mass Spectrometry
Mass Spectrometry on Internet
Index
Preface
Introduction
Principles
5.

図書
図書
5. Schaum's outline of theory and problems of discrete mathematics. 3rd ed.
Seymour Lipschutz, Marc Lars Lipson
出版情報: New York : McGraw-Hill, c2007  xi, 474 p. ; 28 cm
シリーズ名: Schaum's outline series
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Set Theory / Chapter 1：
Relations / Chapter 2：
Functions and Algorithms / Chapter 3：
Logic and Propositional Calculus / Chapter 4：
Techniques of Counting / Chapter 5：
Advanced Counting Techniques, Recursion / Chapter 6：
Probability / Chapter 7：
Graph Theory / Chapter 8：
Directed Graphs / Chapter 9：
Binary Trees / Chapter 10：
Properties of the Integers / Chapter 11：
Languages, Automata, Grammars / Chapter 12：
Finite State Machines and Turing Machines / Chapter 13：
Ordered Sets and Lattices / Chapter 14：
Boolean Algebra / Chapter 15：
Vectors and Matrices / Appendix A：
Algebraic Systems / Appendix B：
Index
Set Theory / Chapter 1：
Relations / Chapter 2：
Functions and Algorithms / Chapter 3：
6.

図書
図書
6. TIP enhancement. 1st ed
edited by Satoshi Kawata, Vladimir M. Shalaev
出版情報: Amsterdam ; Tokyo : Elsevier, 2007  xiv, 323 p. ; 24 cm
シリーズ名: Advances in nano-optics and nano-photonics
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List of Contributors
Preface
Plasmonic materials for surface-enhanced and tip-enhanced Raman spectroscopy / M.A. Young ; J. A. Dieringer ; R.P. Van DuyneChapter 1：
Introduction / [Section] 1：
Nanosphere lithography / [Section] 2：
Size- and shape-tunable localized surface plasmon resonance spectra / [Section] 3：
Fundamentals of localized surface plasmon resonance spectroscopy / [Section] 4：
Electrodynamic calculations / [Section] 5：
The distance dependence of the localized surface plasmon resonance / [Section] 6：
Surface-enhanced Raman spectroscopy / [Section] 7：
Wavelength-scanned surface-enhanced Raman excitation spectroscopy / [Section] 8：
SERS enhancement factor calculation / [Section] 9：
SERS distance dependence by atomic layer deposition / [Section] 10：
2D correlation analysis of SMSERS and single nanoparticle SERS data / [Section] 11：
Tip-enhanced Raman scattering / [Section] 12：
TERS force dependence using AFM / [Section] 13：
Conclusion and outlook / [Section] 14：
Acknowledgments
References
Towards single molecule sensitivity in surface-enhanced Raman scattering / M. Futamata ; Y. MaruyamaChapter 2：
Experiments and numerical analysis
Experimental set up for SERS measurement / 2.1：
Ag nanoparticles preparation / 2.1.1：
Numerical analysis of the local electric field and elastic scattering spectra for metal nanostructures / 2.2：
Results and discussion
Hot particles in SERS / 3.1：
Local field evaluation on the Ag nanoparticles / 3.2：
Origin of the blinking / 3.3：
Blinking at room temperature / 3.3.1：
Blinking at low temperature / 3.3.2：
Critical importance of the junction for SMS-SERS / 3.4：
Elastic scattering experiments / 3.4.1：
Numerical simulations of elastic scattering spectra / 3.4.2：
Emission spectra / 3.5：
Summary
Acknowledgment
Near-field effects in tip-enhanced Raman scattering / Y. Inouye ; P. Verma ; T. Ichimura ; S. KawataChapter 3：
Tip enhancement of Raman scattering
Metallic probe as a nanolight source
Enhancement mechanism for Rhodamine 6G
RRS and SERRS spectra of R6G
TERS spectra of R6G
Near-field Raman scattering from Carbon-60
The gap-mode enhancement / 4.1：
Tip-force effect on C60 / 4.2：
Tip-enhanced nonlinear optical spectroscopy
Photon confinement due to nonlinear optical effect / 5.1：
Tip-enhanced coherent anti-Stokes Raman scattering / 5.2：
Experimental system / 5.3：
Tip-enhanced CARS images of DNA clusters / 5.4：
Conclusion
Use of tip-enhanced vibrational spectroscopy for analytical applications in chemistry, biology, and materials science / T. Schmid ; B.-S. Yeo ; W. Zhang ; R. ZenobiChapter 4：
Setups for tip-enhanced vibrational spectroscopy
Tip-enhanced Raman spectroscopy (TERS)
Tip-enhanced coherent anti-Stokes Raman scattering (TE-CARS)
Scattering scanning near-field optical microscopy (s-SNOM) / 2.3：
Tip fabrication / 2.4：
Enhancement factors and lateral resolution
TERS contrasts and enhancement factors
Comparison of TERS contrasts and enhancement factors
Lateral resolution in apertureless near-field microscopy
Chemical applications
Dyes
Catalysis
Microfluidics and chromatography / 4.3：
Biological applications
Biopolymers
Viruses and biological tissues
Applications in materials science
Nanotubes / 6.1：
Material-specific mapping / 6.2：
Semiconductors / 6.3：
SERS substrates / 6.4：
Conclusions and outlook
Tip-enhanced optical spectroscopy of single-walled carbon nanotubes / A. Hartschuh ; H. Qian ; A.J. Meixner ; N. Anderson ; L. NovotnyChapter 5：
Experimental setup
Single-walled carbon nanotubes
Near-field Raman spectroscopy of SWCNTs
Near-field photoluminescence spectroscopy of SWCNTs
Discussion of the signal enhancement and the image contrast
Scanning nano-Raman spectroscopy of silicon and other semiconducting materials / D. Mehtani ; N. Lee ; R.D. Hartschuh ; A. Kisliuk ; M.D. Foster ; A.P. Sokolov ; J.F. MaguireChapter 6：
Side-illumination geometry and preparation of tips
Apparent enhancement and its localization
Tip enhancement and contrast
Improving contrast for silicon
Optical properties of the apertureless tips
Summary and outlook
Near-field optical structuring and manipulation based on local field enhancement in the vicinity of metal nano structures / R. BachelotChapter 7：
Introduction: context and motivation
General consideration on the optics of metal nanostructures
Tip-enhanced optical lithography (TEOL)
TEOL on inorganic material
TEOL on photopolymer
NFOL based on localized 3-D surface plasmons
Mask-based surface plasmon lithography
Apertureless near-field microscopy of second-harmonic generation / A. V. ZayatsChapter 8：
Second-harmonic generation imaging with SNOM
SHG in the presence of a probe tip
SHG from a probe tip: a localized light source
Tip-enhanced surface SHG
Self-consistent model of second-harmonic ASNOM
Second-harmonic ASNOM: experimental realisation
SHG enhancement at conical objects
SHG from a metal tip apex
SHG ASNOM applications for functional materials characterisation
Resonant optical antennas and single emitters / B. Hecht ; P. Muhlschlegel ; J.N. Farahani ; H.-J. Eisler ; D.W. PohlChapter 9：
Antenna basics
Field enhancement in resonant dipole antennas
Emission of radiation from dipole antennas
Antenna equivalent circuit / 2.2.1：
Antenna impedance / 2.2.2：
True current distribution in a thin dipole antenna / 2.2.3：
Antennas for light
Light confinement by resonant dipole antennas
Nonplasmonic optical antenna / 3.2.1：
Plasmonic optical antenna / 3.2.2：
Light confinement by a resonant bowtie antenna
Fabrication and characterization of resonant optical antennas
Single dipole emitters coupled to optical antennas
Properties of single dipole emitters near metal nano structures
Experimental realization: creating an antenna-based super-emitter
Author index
Subject index
List of Contributors
Preface
Plasmonic materials for surface-enhanced and tip-enhanced Raman spectroscopy / M.A. Young ; J. A. Dieringer ; R.P. Van DuyneChapter 1：
7.

図書
図書
7. Plenty of room for biology at the bottom : an introduction to bionanotechnology
Ehud Gazit
出版情報: London : Imperial College Press , Singapore : Distributed by World Scientific, c2007  xiii, 183 p. ; 24 cm
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Preface
Introduction: Nanobiotechnology and Bionanotechnology / 1：
Classical Biotechnology: Industrial Production Using Biological Systems / 1.1：
Modern Biotechnology: From Industrial Processes to Novel Therapeutics / 1.2：
Modern Biotechnology: Immunological, Enzymatic, and Nucleic Acids-Based Technology / 1.3：
The Interface Between Nanotechnological and Biotechnology: Bionanotechnology / 1.4：
Supramolecular (Bio)Chemistry: The Theoretical Basis for Self-Assembly / 1.5：
The Next Steps for Self-Association at the Nano-Scale / 1.6：
Biology in Nanotechnology and Nano-Sciences in Biotechnology / 1.7：
The Combination of Bionanotechnology and Nanobiotechnology / 1.8：
Nanobionics and Bio-Inspired Nanotechnology / 1.9：
A Brief Introduction to Nanotechnology / 2：
The Emergence of Nanotechnology: "There's Plenty of Room at the Bottom" / 2.1：
Coining the Term "Nanotechnology" and Emergence of the Nanotechnology Concept / 2.2：
Manipulating Molecules: The Scanning Probe Microscopes / 2.3：
Carbon Fullerene: A New Form of Carbon / 2.4：
Carbon Nanotubes: Key Building Blocks for Future Nanotechnological Applications / 2.5：
Non-Carbon Nanotubes and Fullerene-Like Material: The Inorganic Nanomaterials / 2.6：
Quantum Dots and Other Nano-Particles / 2.7：
Nanowires, Nanorods, and Other Nanomaterials / 2.8：
Magnetic Nanoparticles / 2.9：
Natural Biological Assembly at the Nano-Scale / 3：
The Process of Self-Assembly and Self-Organization in Biology / 3.1：
Organization of Bacterial S-Layers / 3.2：
Self-Organization of Viruses / 3.3：
Self-Organization of Phospholipids Membranes / 3.4：
Fibrillar Cytoskeleton Assemblies / 3.5：
Nucleic Acids: The Genetic Information Media and a Template for Nanotechnological Applications / 3.6：
Oligosaccharides and Polysaccharides: Another Class of Biological Polymers / 3.7：
Amyloid Fibrils as Self-Assembled Nano-Scale Bio-Assemblies / 3.8：
Silk: Natural Fibrillar Supramolecular Protein Assembly / 3.9：
Ribosome: The Protein Assembly Line Instrument / 3.10：
Other Complex Machines in the Genetic Code Expression / 3.11：
Protein Quality-Control Machinery: The Proteosome / 3.12：
Biological Nano-Motors: Kinesin and Dynein / 3.13：
Other Nano-Motors: Flagella and Cilia / 3.14：
Ion Channels: Nano-Pores of High Specificity / 3.15：
Nanometric Biological Assemblies: Molecular and Chemical Basis for Interaction / 4：
Emergence of Biological Activity Through Self-Assembly / 4.1：
Molecular Recognition and Chemical Affinity / 4.2：
Affinity and Specificity of Biological Interactions / 4.3：
The Relation Between Thermodynamics and Kinetics of Dissociation / 4.4：
The Chemical Basis for Molecular Recognition and Specific Binding / 4.5：
The Formation Specific Complexes by an Increase in Entropy / 4.6：
Molecular Recognition and the Formation of Biological Structures / 5：
Antibodies as the Molecular Sensors of Recognition / 5.1：
Selection of Antibodies and Equivalent Systems in the Test Tube / 5.2：
Recognition Between Nucleic Acids by Proteins / 5.3：
Interaction Between Receptors and Ligands / 5.4：
Molecular Recognition Between Nucleic Acids / 5.5：
Self-Assembly of Biological and Bio-Inspired Nano-Materials / 6：
Formation of DNA-Based Materials / 6.1：
Peptide-Based Nanomaterials / 6.2：
The First Peptide Nanotubes / 6.3：
Amphiphile and Surfactant-Like Peptide Building-Blocks / 6.4：
Charge Complementary as a Driven Force for Self-Assembly / 6.5：
Conjugation of Peptides for Self-Assembly / 6.6：
Aromatic Interactions for the Formation of Nanostructures / 6.7：
The Formation of Aromatic Dipeptide Nanotubes (ADNT) / 6.8：
The Formation of Spherical Nanostructures by Short Peptides / 6.9：
Peptide Nucleic Acid (PNA) / 6.10：
Application of Biological Assemblies in Nanotechnology / 7：
The Use of S-Layer for Nanolithography / 7.1：
The Use of DNA for Fabrication of Conductive Nanowires / 7.2：
Amyloid Fibrils as Templates for Nanowires Fabrication / 7.3：
Metallization of Actin Filaments by Chemical Modification / 7.4：
The Use of Aromatic Peptide Nanotubes / 7.5：
Bacteriophages as Novel Biomaterials / 7.6：
The Use of Peptide Template for Biomineralization / 7.7：
Production of Inorganic Composite Nanomaterial / 7.8：
The Utilization of Biomineralization in Nanotechnology / 7.9：
Medical and Other Applications of Bionanotechnology / 8：
The Use of Drug Nanocrystals for Improved Application / 8.1：
The Use of Nano-Containers for Drug Delivery / 8.2：
The Use of Inorganic Nanowires for Biological Detection / 8.3：
The Use of Soft Lithography for Biotechnology / 8.4：
Contrast Agents by Nanomagnetic Materials / 8.5：
Nanoagriculture / 8.6：
Water Technology and Nanotechnology / 8.7：
Nanocosmetics / 8.8：
Solar Energy Applications / 8.9：
Future Prospects for Nanobiotechnology and Bionanotechnology / 9：
The Marriage of Molecular Biology and Nanotechnology / 9.1：
The Engineering of Modified Biological Systems for the Assembly of Nanostructures / 9.2：
Nanotechnology and Tissue Engineering / 9.3：
Engineering of the Brain Tissue / 9.4：
Making Artificial Biological Inorganic Composites / 9.5：
Nanobio Machines and Nanorobots / 9.6：
Concluding Remarks: The Prospects and Dangers of the Nanobiological Revolution / 10：
There's Plenty of Room at the Bottom: An Invitation to Enter a New Field of Physics - by Richard P. Feynman / Appendix A：
List of Bionanotechnological and Nanobiotechnological Companies / Appendix B：
Glossary / Appendix C：
Bibliography
Index
Preface
Introduction: Nanobiotechnology and Bionanotechnology / 1：
Classical Biotechnology: Industrial Production Using Biological Systems / 1.1：
8.

図書
図書
8. The world without us
Alan Weisman
出版情報: New York : Thomas Dunne Books, c2007  viii, 324 p. ; 25 cm
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9.

図書
図書
9. More concepts and applications
edited by Chad A. Mirkin and Christof M. Niemeyer
出版情報: Weinheim : Wiley-VCH, c2007  xxvi, 432 p. ; 25 cm
シリーズ名: Nanobiotechnology / edited by Christof M. Niemeyer and Chad A. Mirkin ; 2
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10.

図書
図書
10. Nanomaterials for biosensors
edited by Challa S.S.R. Kumar
出版情報: Weinheim : Wiley-VCH, c2007  xxi, 408 p. ; 25 cm
シリーズ名: Nanotechnologies for the life sciences ; v. 8
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Preface
List of Authors
Biosensing using Carbon Nanotube Field-effect Transistors / Padmakar D. Kichambare ; Alexander Star1：
Overview / 1.1：
Introduction / 1.2：
Carbon Nanotube Field-effect Transistors (NTFETs) / 1.3：
Sensor Applications of NTFETs / 1.4：
Conclusion and Outlook / 1.5：
Carbon Nanotube-based Sensor / Jian-Shan Ye ; Fwu-Shan Sheu2：
Introduction of Carbon Nanotubes / 2.1：
Growth of Carbon Nanotubes / 2.3：
Methods to Prepare CNTs-based Sensors and Biosensors / 2.4：
Application of CNTs-based Electrochemical Sensors and Biosensors / 2.5：
Functionalization of CNTs / 2.6：
Conclusions and Future Prospects / 2.7：
Nanotubes, Nanowires, and Nanocantilevers in Biosensor Development / Jun Wang ; Guodong Liu ; Yuehe Lin3：
Carbon Nanotubes in Biosensor Development / 3.1：
Nanowires in Biosensor Development / 3.3：
Nanocantilevers for Biosensors / 3.4：
Summary / 3.5：
Fullerene-based Electrochemical Detection Methods for Biosensing / Nikos Chaniotakis4：
Aims of the Chapter / 4.1：
Electrochemical Biosensing / 4.3：
Evolution of Biosensors / 4.4：
Mediation Process in Biosensors / 4.5：
Fullerenes / 4.6：
Fullerene-mediated Biosensing / 4.7：
Conclusions / 4.8：
Optical Biosensing Based on Metal and Semiconductor Colloidal Nanocrystals / Roberto Comparelli ; Maria Lucia Curri ; Pantaleo Davide Cozzoli ; Marinella Striccoli5：
Colloidal Nanocrystals / 5.1：
Nanocrystal Functionalization for Biosensing / 5.4：
Optical Techniques / 5.5：
Advantages and Disadvantages of Nanocrystals in Optical Detection / 5.6：
Applications / 5.7：
Towards Marketing / 5.8：
Quantum Dot-based Nanobiohybrids for Fluorescent Detection of Molecular and Cellular Biological Targets / Zhivko Zhelev ; Rumiana Bakalova ; Hideki Ohba ; Yoshinobu Baba5.9：
Quantum Dots - Basic Principles of Design and Synthesis, Optical Properties, and Advantages over Classical Fluorophores / 6.1：
Quantum Dots for Fluorescent Labeling and Imaging / 6.3：
Quantum Dots for Immunoblot Analysis with Fluorescent Detection / 6.4：
Quantum Dots for FRET Analyses, Time-resolved Fluorimetry, and Development of Optical Recognition-based Biosensors / 6.5：
Quantum Dots as New Fluorescent Standards for the Thin Calibration of Fluorescent Instrumentation / 6.6：
Detection of Biological Materials by Gold Nano-biosensor-based Electrochemical Method / Juan Jiang ; Manju Basu ; Sara Seggerson ; Albert Miller ; Michael Pugia ; Subhash Basu7：
Template Synthesis of Gold Nano-wire Arrays for Biosensor Applications / 7.1：
Synthesis of a Linker and its Attachment to Gold Posts of GNW followed by Binding to Specific Antibodies / 7.3：
Development of Electrochemical Nano-biosensor for Bacteria Detection / 7.4：
Dendrimer-based Electrochemical Detection Methods / Hak-Sung Kim ; Hyun C. Yoon7.5：
Applications for Biosensor / 8.1：
Preface
List of Authors
Biosensing using Carbon Nanotube Field-effect Transistors / Padmakar D. Kichambare ; Alexander Star1：
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