close
1.

図書

図書
edited by David Barry ... [et al.]
出版情報: Wymondham : Horizon Bioscience, c2007  xi, 423 p. ; 24 cm
所蔵情報: loading…
2.

図書

図書
Erich Steiner
出版情報: Oxford ; New York : Oxford University Press, 2008  xii, 668 p. ; 25 cm
所蔵情報: loading…
目次情報: 続きを見る
Numbers, variables, and units / 1:
Concepts / 1.1:
Real numbers / 1.2:
Factorization, factors, and factorials / 1.3:
Decimal representation of numbers / 1.4:
Variables / 1.5:
The algebra of real numbers / 1.6:
Complex numbers / 1.7:
Units / 1.8:
Exercises / 1.9:
Algebraic functions / 2:
Graphical representation of functions / 2.1:
Factorization and simplification of expressions / 2.3:
Inverse functions / 2.4:
Polynomials / 2.5:
Rational functions / 2.6:
Partial fractions / 2.7:
Solution of simultaneous equations / 2.8:
Transcendental functions / 2.9:
Trigonometric functions / 3.1:
Inverse trigonometric functions / 3.3:
Trigonometric relations / 3.4:
Polar coordinates / 3.5:
The exponential function / 3.6:
The logarithmic function / 3.7:
Values of exponential and logarithmic functions / 3.8:
Hyperbolic functions / 3.9:
Differentiation / 3.10:
The process of differentiation / 4.1:
Continuity / 4.3:
Limits / 4.4:
Differentiation from first principles / 4.5:
Differentiation by rule / 4.6:
Implicit functions / 4.7:
Logarithmic differentiation / 4.8:
Successive differentiation / 4.9:
Stationary points / 4.10:
Linear and angular motion / 4.11:
The differential / 4.12:
Integration / 4.13:
The indefinite integral / 5.1:
The definite integral / 5.3:
The integral calculus / 5.4:
Uses of the integral calculus / 5.5:
Static properties of matter / 5.6:
Dynamics / 5.7:
Pressure-volume work / 5.8:
Methods of integration / 5.9:
The use of trigonometric relations / 6.1:
The method of substitution / 6.3:
Integration by parts / 6.4:
Reduction formulas / 6.5:
Rational integrands. The method of partial fractions / 6.6:
Parametric differentiation of integrals / 6.7:
Sequences and series / 6.8:
Sequences / 7.1:
Finite series / 7.3:
Infinite series / 7.4:
Tests of convergence / 7.5:
MacLaurin and Taylor series / 7.6:
Approximate values and limits / 7.7:
Operations with power series / 7.8:
Algebra of complex numbers / 7.9:
Graphical representation / 8.3:
Complex functions / 8.4:
Euler's formula / 8.5:
Periodicity / 8.6:
Evaluation of integrals / 8.7:
Functions of several variables / 8.8:
Partial differentiation / 9.1:
The total differential / 9.4:
Some differential properties / 9.6:
Exact differentials / 9.7:
Line integrals / 9.8:
Multiple integrals / 9.9:
The double integral / 9.10:
Change of variables / 9.11:
Functions in 3 dimensions / 9.12:
Spherical polar coordinates / 10.1:
Functions of position / 10.3:
Volume integrals / 10.4:
The Laplacian operator / 10.5:
Other coordinate systems / 10.6:
First-order differential equations / 10.7:
Solution of a differential equation / 11.1:
Separable equations / 11.3:
Separable equations in chemical kinetics / 11.4:
First-order linear equations / 11.5:
An example of linear equations in chemical kinetics / 11.6:
Electric circuits / 11.7:
Second-order differential equations. Constant coefficients / 11.8:
Homogeneous linear equations / 12.1:
The general solution / 12.3:
Particular solutions / 12.4:
The harmonic oscillator / 12.5:
The particle in a one-dimensional box / 12.6:
The particle in a ring / 12.7:
Inhomogeneous linear equations / 12.8:
Forced oscillations / 12.9:
Second-order differential equations. Some special functions / 12.10:
The power-series method / 13.1:
The Frobenius method / 13.3:
The Legendre equation / 13.4:
The Hermite equation / 13.5:
The Laguerre equation / 13.6:
Bessel functions / 13.7:
Partial differential equations / 13.8:
General solutions / 14.1:
Separation of variables / 14.3:
The particle in a rectangular box / 14.4:
The particle in a circular box / 14.5:
The hydrogen atom / 14.6:
The vibrating string / 14.7:
Orthogonal expansions. Fourier analysis / 14.8:
Orthogonal expansions / 15.1:
Two expansions in Legendre polynomials / 15.3:
Fourier series / 15.4:
Fourier transforms / 15.5:
Vectors / 15.7:
Vector algebra / 16.1:
Components of vectors / 16.3:
Scalar differentiation of a vector / 16.4:
The scalar (dot) product / 16.5:
The vector (cross) product / 16.6:
Scalar and vector fields / 16.7:
The gradient of a scalar field / 16.8:
Divergence and curl of a vector field / 16.9:
Vector spaces / 16.10:
Determinants / 16.11:
Determinants of order 3 / 17.1:
The general case / 17.3:
The solution of linear equations / 17.4:
Properties of determinants / 17.5:
Reduction to triangular form / 17.6:
Alternating functions / 17.7:
Matrices and linear transformations / 17.8:
Some special matrices / 18.1:
Matrix algebra / 18.3:
The inverse matrix / 18.4:
Linear transformations / 18.5:
Orthogonal matrices and orthogonal transformations / 18.6:
Symmetry operations / 18.7:
The matrix eigenvalue problem / 18.8:
The eigenvalue problem / 19.1:
Properties of the eigenvectors / 19.3:
Matrix diagonalization / 19.4:
Quadratic forms / 19.5:
Complex matrices / 19.6:
Numerical methods / 19.7:
Errors / 20.1:
Solution of ordinary equations / 20.3:
Interpolation / 20.4:
Numerical integration / 20.5:
Methods in linear algebra / 20.6:
Gauss elimination for the solution of linear equations / 20.7:
Gauss-Jordan elimination for the inverse of a matrix / 20.8:
Systems of differential equations / 20.9:
Probability and statistics / 20.11:
Descriptive statistics / 21.1:
Frequency and probability / 21.3:
Combinations of probabilities / 21.4:
The binomial distribution / 21.5:
Permutations and combinations / 21.6:
Continuous distributions / 21.7:
The Gaussian distribution / 21.8:
More than one variable / 21.9:
Least squares / 21.10:
Sample statistics / 21.11:
Standard integrals / 21.12:
Solutions to exercises
Index
Numbers, variables, and units / 1:
Concepts / 1.1:
Real numbers / 1.2:
3.

図書

図書
by Megumi Fujii
出版情報: New York : Vertical, c2007  79 p. ; 26 cm
所蔵情報: loading…
4.

図書

図書
Hossein Agheli
出版情報: Saarbrücken : VDM Verlag Dr. Müller, c2008  79 p. ; 23 cm
所蔵情報: loading…
5.

図書

図書
Jennifer J. Deal and Don W. Prince
出版情報: Greensboro, N.C. : Center for Creative Leadership, c2003  31 p. ; 23 cm
シリーズ名: An ideas into action guidebook
所蔵情報: loading…
6.

図書

図書
edited by François Baneyx
出版情報: Wymondham : Horizon Bioscience, c2004  x, 532 p. ; 25 cm
所蔵情報: loading…
7.

図書

図書
David S. Kidder & Noah D. Oppenheim
出版情報: New York : Rodale : Distributed to the book trade by Holtzbrinck Publishers, c2006  377 p. ; 21 cm
所蔵情報: loading…
8.

図書

図書
edited by Eric G. Derouane
出版情報: Chichester : J. Wiley & Sons, c2006  xii, 243 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 4
所蔵情報: loading…
目次情報: 続きを見る
Series Preface
Preface to Volume 4
Abbreviations
An Overview of Zeolite, Zeotype and Mesoporous Solids Chemistry: Design, Synthesis and Catalytic Properties / Thomas Maschmeyer ; Leon van de Water1:
Zeolites, zeotypes and mesoporous solids: synthetic aspects / 1.1:
Introduction / 1.1.1:
Synthetic aspects: template theory for zeolite synthesis / 1.1.2:
Synthetic aspects: template theory for mesoporous oxides synthesis / 1.1.3:
Design of extra-large pore zeolites and other micro- and mesoporous catalysts / 1.2:
Extra-large pore zeolites / 1.2.1:
Hierarchical pore architectures: combining micro- and mesoporosity / 1.2.3:
Potential of post-synthesis functionalized micro- and mesoporous solids as catalysts for fine chemical synthesis / 1.3:
Covalent functionalization / 1.3.1:
Noncovalent immobilization approaches / 1.3.3:
Single-site catalysts inspired by natural systems / 1.3.4:
References
Problems and Pitfalls in the Applications of Zeolites and other Microporous and Mesoporous Solids to Catalytic Fine Chemical Synthesis / Michel Guisnet ; Matteo Guidotti2:
Zeolite catalysed organic reactions / 2.1:
Fundamental and practical differences with homogeneous reactions / 2.2.1:
Batch mode catalysis / 2.2.2:
Continuous flow mode catalysis / 2.2.3:
Competition for adsorption: influence on reaction rate, stability and selectivity / 2.2.4:
Catalyst deactivation / 2.2.5:
General conclusions / 2.3:
Aromatic Acetylation / 3:
Aromatic acetylation / 3.1:
Acetylation with Acetic Anhydride / 3.1.1:
Acetylation with Acetic Acid / 3.1.2:
Procedures and protocols / 3.2:
Selective synthesis of acetophenones in batch reactors through acetylation with acetic anhydride / 3.2.1:
Selective synthesis of acetophenones in fixed bed reactors through acetylation with acetic anhydride / 3.2.2:
Aromatic Benzoylation / Patrick Geneste ; Annie Finiels4:
Aromatic benzoylation / 4.1:
Effect of the zeolite / 4.1.1:
Effect of the acylating agent / 4.1.2:
Effect of the solvent / 4.1.3:
Benzoylation of phenol and the Fries rearrangement / 4.1.4:
Kinetic law / 4.1.5:
Substituent effect / 4.1.6:
Experimental / 4.1.7:
Acylation of anisole over mesoporous aluminosilicates / 4.2:
Nitration of Aromatic Compounds / Avelino Corma ; Sara Iborra5:
Reaction mechanism / 5.1:
Nitration of aromatic compounds using zeolites as catalysts / 5.3:
Nitration in liquid phase / 5.3.1:
Vapour phase nitration / 5.3.2:
Conclusions / 5.4:
Oligomerization of Alkenes / 6:
Reaction mechanisms / 6.1:
Acid zeolites as catalysts for oligomerization of alkenes / 6.3:
Medium pore zeolites: influence of crystal size and acid site density / 6.3.1:
Use of large pore zeolites / 6.3.2:
Catalytic membranes for olefin oligomerization / 6.3.3:
Mesoporous alominosilicates as oligomerization catalysts / 6.4:
Nickel supported aluminosilicates as catalysts / 6.5:
Microporous and Mesoporous Catalysts for the Transformation of Carbohydrates / Claude Moreau7:
Hydrolysis of sucrose in the presence of H-form zeolites / 7.1:
Hydrolysis of fructose and glucose precursors / 7.3:
Isomerization of glucose into fructose / 7.4:
Dehydration of fructose and fructose-precursors / 7.5:
Dehydration of xylose / 7.6:
Synthesis of alkyl-D-glucosides / 7.7:
Synthesis of butyl-D-glucosides / 7.7.1:
Synthesis of long-chain alkyl-D-glucosides / 7.7.2:
Synthesis of alkyl-D-fructosides / 7.8:
Hydrogenation of glucose / 7.9:
Oxidation of glucose / 7.10:
One-pot Reactions on Bifunctional Catalysts / 7.11:
Examples / 8.1:
One-pot transformations involving successive hydrogenation and acid-base steps / 8.2.1:
One-pot transformations involving successive oxidation and acid-base steps / 8.2.2:
Base-type Catalysts / Didier Tichit ; Daniel Brunel9:
Characterization of solid bases / 9.1:
Test reactions / 9.2.1:
Probe molecules combined with spectroscopic methods / 9.2.2:
Solid base catalysts / 9.3:
Alkaline earth metal oxides / 9.3.1:
Catalysis on alkaline earth metal oxides / 9.3.2:
Hydrotalcites and related compounds / 9.3.3:
Organic base-supported catalysts / 9.3.4:
Hybrid Oxidation Catalysts from Immobilized Complexes on Inorganic Microporous Supports / Dirk De Vos ; Ive Hermans ; Ben Sels ; Pierre Jacobs9.4:
Introduction and scope / 10.1:
Oxygenation potential of heme-type complexes in zeolite / 10.2:
Metallo-phthallocyanines encapsulated in the cages of faujasite-type zeolites / 10.2.1:
Oxygenation potential of metallo-phthallocyanines encapsulated in the mesopores of VPI-5 AIPO[subscript 4] / 10.2.2:
Oxygenation potential of zeolite encapsulated metallo-porphyrins / 10.2.3:
Oxygenation potential of zeolite encapsulated nonheme complexes / 10.3:
Immobilization of N,N[prime]-bidentate complexes in zeolite Y / 10.3.1:
Ligation of zeolite exchanged transition ions with bidentate aza ligands / 10.3.2:
Ligation of zeolite exchanged transition ions with tri- and tetra-aza(cyclo)alkane ligands / 10.3.3:
Ligation of zeolite exchanged transition ions with Schiff base-type ligands / 10.3.4:
Zeolite effects with N,N[prime]-bis(2-pyridinecarboxamide) complexes of Mn and Fe in zeolite Y / 10.3.5:
Zeolite encapsulated chiral oxidation catalysts / 10.3.6:
Acknowledgements / 10.4:
Subject Index
Series Preface
Preface to Volume 4
Abbreviations
9.

図書

図書
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
所蔵情報: loading…
目次情報: 続きを見る
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
10.

図書

図書
edited by Cecilia Heyes and Ludwig Huber
出版情報: Cambridge, Mass. : MIT Press, c2000  viii, 386 p. ; 24 cm
シリーズ名: Bradford book
Vienna series in theoretical biology
所蔵情報: loading…
文献の複写および貸借の依頼を行う
 文献複写・貸借依頼