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1.

図書

図書
J.A. Joule, Keith Mills
出版情報: Chichester : Wiley, 2010  xxviii, 689 p. ; 25 cm
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Preface
Definitions of abbreviations
Heterocyclic nomenclature / 1:
Structures and spectroscopic properties of aromatic heterocycles / 2:
Substitutions of aromatic heterocycles / 3:
Organometallic heterocyclic chemistry / 4:
Methods in heterocyclic chemistry / 5:
Ring synthesis of aromatic heterocycles / 6:
Typical reactivity of pyridines, quinolines and isoquinolines / 7:
Pyridines: reactions and synthesis / 8:
Quinolines and isoquinolines: reactions and synthesis / 9:
Typical reactivity of pyrylium and benzopyrylium ions, pyrones and benzopyrones / 10:
Pyryliums, 2- and 4-pyrones: reactions and synthesis / 11:
Benzopyryliums, benzopyrones: reactions and synthesis / 12:
Typical reactivity of the diazines: pyridazine, pyrimidine and pyrazine / 13:
The diazines: pyridazine, pyrimidine, and pyrazine: reactions and synthesis / 14:
Typical reactivity of pyrroles, thiophenes, and furans / 15:
Pyrroles: reactions and synthesis / 16:
Thiophenes: reactions and synthesis / 17:
Furans: reactions and synthesis / 18:
Typical reactivity of indoles, benzo[b]thiophenes, benzo[b]furans, isoindoles, benzo[c]thiophenes and isobenzofurans / 19:
Indoles: reactions and synthesis / 20:
Benzo[b]thiophenes and benzo[b]furans: reactions and synthesis / 21:
Isoindoles, benzo[c]thiophenes and isobenzofurans: reactions and synthesis / 22:
Typical reactivity of 1,3- and 1,2-azoles and benzo-1,3- and -1,2-azoles / 23:
1,3-Azoles: imidazoles, thiazoles, and oxazoles: reactions and synthesis / 24:
1,2-Azoles: pyrazoles, isothiazoles, isoxazoles: reactions and synthesis / 25:
Benzanellated azoles: reactions and synthesis / 26:
Purines: reactions and synthesis / 27:
Heterocycles containing a ring-junction nitrogen / bridgehead compounds28:
Heterocycles containing more than two heteroatoms / 29:
Saturated and partially unsaturated heterocyclic compounds: reactions and synthesis / 30:
Special topics / 31:
Heterocycles in biochemistry theterocyclic natural products / 32:
Heterocycles in medicine / 33:
Heterocycles containing a ring-junction nitrogen (bridgehead compounds)
Preface
Definitions of abbreviations
Heterocyclic nomenclature / 1:
2.

図書

図書
John A. Joule, Keith Mills著 ; 中川昌子, 有澤光弘訳
出版情報: 東京 : 東京化学同人, 2016.2  xvi, 238p ; 26cm
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ヘテロ環化合物の命名
芳香族ヘテロ環化合物の構造
ヘテロ環の一般的化学反応性
ヘテロ環化学におけるパラジウム
ピリジン
ジアジン
キノリンとイソキノリン
ピリリウム、ベンゾピリリウム、ピロン、ベンゾピロン
ピロール
インドール
フランとチオフェン
1,2アゾールと1,3アゾール
プリン
五員環 : とアジン / 六員環
還縮合位に窒素をもつヘテロ環
非芳香族へテロ環
天然に見いだされるヘテロ環
医薬品にみるヘテロ環
日常生活にみるヘテロ環
ヘテロ環化合物の命名
芳香族ヘテロ環化合物の構造
ヘテロ環の一般的化学反応性
3.

図書

図書
editors, H. Suschitzky and E.F.V. Scriven
出版情報: Oxford ; New York, N.Y. : Pergamon Press, 1989-  v. ; 23-25 cm
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Chapter headings: Substituted Heterocyclic Compounds by Selective Control of Halogen-Dance Reactions / J. Frohlich
Heterocycles as Vehicles for Synthesis / A. Padwa
Three-Membered Ring Systems / S.S. Murphree
Four-Membered Ring Systems / J. Parrick ; L.K. Mehta
Five-Membered Ring Systems
Six-Membered Ring Systems
Seven-Membered Rings / M. Balasubramanian
Eight-Membered and Larger Rings / G.R. Newkome
Subject Index
Chapter headings: Polyfunctionalized Pyrroles and Pyrazoles from Conjugated Azoalkenes
Application of Diels-Alder Cycloaddition Chemistry for Heterocyclic Synthesis
Subject index
Foreword
Editorial Advisory Board Members
Recent Advances in the Synthesis of Heterocycles via Ring-Closing Metathesis / Michael A. WaltersChapter 1:
Chapter headings
The Junjappa-Ila JI)-heteroaromatic annulation / Chapter 2:
The synthesis of fused 7-azanorbornanes / James W. Pavlik
Three-membered ring systems
Four-membered ring systems
Photochemical Isomerizations of Some Five-Membered Heteroaromatic Azoles
Five-membered ring systems
Six-membered ring systems / Chapter 3:
Seven-membered rings / Gordon W. Gribble
Eight-membered and larger rings
Naturally Occurring Halogenated Pyrroles and Indoles
Three- and Four-Membered Ring Systems / Chapter 4:
Thiophenes & Se, Te Analogs / Albert Padwa ; Shaun Murphree ; Benito Alcaide ; Pedro Almendros ; Erin T. PelkeyPart 1.:
Pyrroles and Benzo Derivatives / Tomasz Janosik ; Jan Bergman
Furans and Benzofurans / Xue-Long Hou ; Zhen Yang ; Henry N. C. WongPart 3.:
With More than One N Atom / Larry YetPart 4.:
With N & S (Se) Atoms / David J. Wilkins ; Paul A. BradleyPart 5.:
With O & S (Se, Te) Atoms / R. Alan Aitken ; Stephen J. CostelloPart 6.:
With O & N Atoms / Stefano Cicchi ; Franca M. Cordero ; Donatella GiomiPart 7.:
Pyridines and Benzo Derivatives / D. Scott Coffey ; Stanley P. Kolis ; Scott A. MayChapter 6:
Diazines and Benzo Derivatives / Michael P. Groziak
Triazines, Tetrazines and Fused Ring Polyaza Systems / Carmen Ochoa ; Pilar Goya
With O and/or S Atoms / John D. Hepworth ; B. Mark Heron
Index / John D. Bremner ; George R. NewkomeChapter 7:
The Synthesis of Oxazoles from Diazocarbronyl Compounds / C.J. Moody ; K.J. Doyle
The Heterocyclic Chemistry Associated with the Herbicide Glyphosate / J.A. Sikorski
Five-Membered Ring Systems. Thiophenes & Se & Te analogs / J. B. Press ; E.T. Pelkey
Pyrroles and benzo derivatives / D.M. Ketcha
Furans and benzo derivatives / S. Reck ; W. Friedrichsen
With more than one N atom / M.A. Walters ; J.R. Vargas
With N & S Se) atoms / P.A. Bradley ; D.J. Wilkins
With O & SSe, Te) atoms / R.A. Aitken ; L. Hill
With O & N atoms / G.V. Boyd
Six-Membered Ring Systems. Pyridine and benzo derivatives / D.L. Comins ; S. O'Connor
Diazines and benzo derivatives / M.P. Groziak
Triazines, tetrazines and fused polyaza systems / D.T. Hurst
With O and/or S atoms / J.D. Hepworth ; B.M. Heron
Geminal Diazides of Heterocycles / D.J. Le Count ; Th. Kappe ; C.O. Kappe
Radical Methods the Synthesis of Heterocyclic Compounds / M.P. Sibi ; J. Ji
Thiophenes & Se & Te Analogs / R.K. Russell ; J.B. Press
Furans and Benzo Derivatives / R.J. Sundberg ; St. Reck
With N and S Se) Atoms / S.A. Lang, Jr ; V.J. Lee ; R. Tanaka
With O & S Se, Te) Atoms
Pyridine and Benzo Derivatives / J.E. Toomey ; R. Murugan
Extrusion of SO 2 from Heterocyclic Compounds, Part 2: Five-Membered Rings
Methyl 2-Benzoylamino-3-Dimethylaminopropenoate in the Synthesis of Heterocyclic Systems
The Diels-Alder cycloadditions of 3,5-dibromo-2-pyrone and its derivatives / Heui-Yeon Kim ; Cheon-Gyu Cho
Overview of the Diels-Alder chemistry of 2-pyrone / 1.1:
3,5-Dibromo-2-pyrone / 1.2:
[4+2] Cycloadditions of 3.5-dibromo-2-pyrone / 1.2.1:
Synthesis and cycloadditions of substituted monobromo-2-pyrones / 1.2.2:
Intramolecular Diels-Alder cycloadditions of 2-pyrones / 1.2.3:
Conclusion / 1.3:
Acknowledgements / 1.4:
References / 1.5:
Recent developments in the chemistry of nucleosides / Jean-Luc Girardet ; Stanley A. Lang
Introduction / 2.1:
Sugar chemistry / 2.2:
Hydrogen and oxygen substitutions / 2.2.1:
Modifications at C-1' / 2.2.1.1:
Modifications at C-2' / 2.2.1.2:
Modifications at C-3' / 2.2.1.3:
Modifications at C-4' / 2.2.1.4:
Modifications at C-5' / 2.2.1.5:
Ring-oxygen substitution / 2.2.2:
Substitution with carbon / 2.2.2.1:
Substitution with sulfur / 2.2.2.2:
Substitution with nitrogen / 2.2.2.3:
Nucleosides with bicyclic sugars / 2.2.3:
Spiro nucleosides / 2.2.3.1:
Bicyclic nucleosides / 2.2.3.2:
Combinatorial approaches / 2.3:
2004 / 2.4:
Epoxides / 3.1.1:
Preparation of epoxides / 3.1.2.1:
Reactions of epoxides / 3.1.2.2:
Aziridines / 3.1.3:
Preparation of aziridines / 3.1.3.1:
Reactions of aziridines / 3.1.3.2:
2005 / Stephen C. Bergmeier ; Damon D. Reed3.1.4:
Azetidines and azetes / 3.2.1:
Monocyclic 2-azetidinones ([beta]-lactams) / 4.3:
Fused polycyclic [beta]-lactams / 4.4:
Oxetanes, dioxetanes, oxetes and 2-oxetanones ([beta]-lactones) / 4.5:
Thietanes, [beta]-sultams, and related systems / 4.6:
Silicon and phosphorus heterocycles. miscellaneous / 4.7:
Thiophenes and Se/Te Analogues / 4.8:
Thiophene ring synthesis / 5.1.1:
Reactions of thiophenes / 5.1.3:
Non-polymeric thiophene organic materials / 5.1.4:
Thiophene oligomers and polymers / 5.1.5:
Thiophene derivatives in medicinal chemistry / 5.1.6:
Selenophenes and tellurophenes / 5.1.7:
Synthesis of pyrroles / 5.1.8:
Intramolecular approaches / 5.2.2.1:
Intermolecular approaches / 5.2.2.2:
Transformation of other heterocycles / 5.2.2.3:
Reactions of pyrroles / 5.2.3:
Substitution at nitrogen / 5.2.3.1:
Substitution at carbon / 5.2.3.2:
Functionalization of the side-chain / 5.2.3.3:
Pyrrole natural products and materials / 5.2.4:
Natural products / 5.2.4.1:
Macrocycles and oligopyrroles / 5.2.4.2:
Non-oligomeric materials / 5.2.4.3:
Synthesis of indoles / 5.2.5:
Oxindoles, azaindoles, and carbazoles / 5.2.5.1:
Reactions of indoles / 5.2.6:
Substitution at C-2/C-3 / 5.2.6.1:
Functionalization of the benzene ring / 5.2.6.3:
Indole natural products / 5.2.6.4:
Furans and benzofurans / Kap-Sun Yeung5.2.7.1:
Reactions / 5.3.1:
Furans / 5.3.2.1:
Di- and tetrahydrofurans / 5.3.2.2:
Synthesis / 5.3.3:
Benzo[b]furans and related compounds / 5.3.3.1:
Benzo[c]furans and related compounds / 5.3.3.4:
With more than One N Atom / 5.3.4:
Pyrazoles and ring-fused derivatives / 5.4.1:
Imidazoles and ring-fused derivatives / 5.4.3:
1,2,3-Triazoles and ring-fused derivatives / 5.4.4:
1,2,4-Triazoles and ring-fused derivatives / 5.4.5:
Tetrazoles and ring-fused derivatives / 5.4.6:
With N and S (Se) atoms / Yong-Jin Wu ; Bingwei V. Yang5.4.7:
Thiazoles / 5.5.1:
Synthesis of thiazoles and fused derivatives / 5.5.2.1:
Synthesis of thiazolines / 5.5.2.2:
Synthesis of 2-imino-thiazolidine and thiazoline derivatives / 5.5.2.3:
Reactions of thiazoles and fused derivatives / 5.5.2.4:
Reactions of thiazolines / 5.5.2.5:
Thiazole intermediates in synthesis / 5.5.2.6:
Thiazolium-catalyzed and-mediated reactions / 5.5.2.7:
Thiazole-containing drug candidates / 5.5.2.9:
New thiazole-containing natural products / 5.5.2.10:
Isothiazoles / 5.5.3:
Synthesis of isothiazoles by ring-formation / 5.5.3.1:
Reactions of isothiazoles / 5.5.3.2:
Isothiazoles as auxiliaries in organic syntheses / 5.5.3.3:
Biologically interesting isothiazoles / 5.5.3.4:
Thiadiazoles and selenadiazoles / 5.5.4:
1,3-Selenazoles, 1,3-selenazolidines and 1,3-tellurazoles / 5.5.5:
With O and S (Se, Te) atoms / Lynn A. Power5.5.6 Acknowledgement:
1,3-Dioxoles and dioxolanes / 5.6.1:
1,3-Dithioles and dithiolanes / 5.6.2:
1,3-Oxathioles and oxathiolanes / 5.6.3:
1,2-Dioxolanes / 5.6.4:
1,2-Dithioles and dithiolanes / 5.6.5:
1,2-Oxathioles and oxathiolanes / 5.6.6:
Three heteroatoms / 5.6.7:
With O and N atoms / 5.6.8:
Isoxazoles / 5.7.1:
Isoxazolines / 5.7.2:
Isoxazolidines / 5.7.3:
Oxazoles / 5.7.4:
Oxazolines / 5.7.5:
Oxazolidines / 5.7.6:
Oxadiazoles / 5.7.7:
Pyridines and benzo derivatives / Heidi L. Fraser ; M. Brawner Floyd ; Darrin W. Hopper5.7.8:
Pyridines / 6.1.1:
Preparation of pyridines / 6.1.2.1:
Reactions of pyridines / 6.1.2.2:
Pyridine N-oxides and pyridinium Salts / 6.1.2.3:
Quinolines / 6.1.3:
Preparation of quinolines / 6.1.3.1:
Reactions of quinolines / 6.1.3.2:
Tsoquinolines / 6.1.4:
Preparation of isoquinolines / 6.1.4.1:
Reactions of isoquinolines / 6.1.4.2:
Piperidines / 6.1.5:
Preparations of piperidines / 6.1.5.1:
Triazines, tetrazines and fused ring polyaza systems / Cristina Gomez de la Oliva6.1.6:
Triazines / 6.3.1:
1,2,3-Triazines / 6.3.1.1:
1,2,4-Triazines / 6.3.1.2:
1,3,5-Triazines / 6.3.1.3:
Tetrazines / 6.3.2:
Fused [6]+[5] polyaza systems / 6.3.3:
Triazino and tetrazino [6+5] fused systems / 6.3.3.1:
Purines and related structures / 6.3.3.2:
Fused [6]+[6] polyaza systems / 6.3.4:
Miscellaneous fused polyaza systems / 6.3.5:
Heterocycles containing one oxygen atom / 6.3.6:
Pyrans / 6.4.2.1:
[1]Benzopyrans and dihydro[1]benzopyrans / 6.4.2.2:
[2]Benzopyrans and dihydro[2]benzopyrans / 6.4.2.3:
Pyrylium Salts / 6.4.2.4:
Pyranones / 6.4.2.5:
Coumarins / 6.4.2.6:
Chromones / 6.4.2.7:
Xanthones and xanthenes / 6.4.2.8:
Heterocycles containing one sulfur atom / 6.4.3:
Thiopyrans and analogues / 6.4.3.1:
Heterocycles containing two or more oxygen atoms / 6.4.4:
Dioxins and dioxanes / 6.4.4.1:
Trioxanes / 6.4.4.2:
Heterocycles containing two or more sulfur atoms / 6.4.5:
Dithianes and trithianes / 6.4.5.1:
Heterocycles containing both oxygen and sulfur in the same ring / 6.4.6:
Oxathianes / 6.4.6.1:
Seven-membered ring systems / John B. Bremner ; Siritron Samosorn6.4.7:
Seven-membered systems containing one heteroatom / 7.1:
Azepines and derivatives / 7.2.1:
Fused azepines and derivatives / 7.2.2:
Oxepines and fused derivatives / 7.2.3:
Thiepines and fused derivatives / 7.2.4:
Seven-membered systems containing two heteroatoms / 7.3:
Diazepines and fused derivatives / 7.3.1:
Dioxepines, dithiepines and fused derivatives / 7.3.2:
Miscellaneous derivatives with two heteroatoms / 7.3.3:
Seven-membered systems containing three or more heteroatoms / 7.4:
Systems with N, S and/or O / 7.4.1:
Seven-membered systems of pharmacological significance / 7.5:
Future directions / 7.6:
Carbon-oxygen rings / 7.7:
Carbon-nitrogen rings / 8.3:
Carbon-sulfur rings / 8.4:
Carbon-silicon rings / 8.5:
Carbon-selenium rings / 8.6:
Carbon-oxygen/carbon-nitrogen rings / 8.7:
Carbon-nitrogen-oxygen rings / 8.8:
Carbon-nitrogen-sulfur rings / 8.9:
Carbon-phosphorus-sulfur rings / 8.10:
Carbon-phosphorus-nitrogen rings / 8.11:
Carbon-selenium-nitrogen rings / 8.12:
Carbon-sulfur-oxygen rings / 8.13:
Carbon-nitrogen-sulfur-oxygen rings / 8.14:
Carbon-nitrogen-metal rings / 8.15:
Carbon-phosphorus-metal rings / 8.16:
Carbon-oxygen-nitrogen-metal rings / 8.17:
Carbon-sulfur-nitrogen-metal rings / 8.18:
Carbon-phosphorus-oxygen-metal rings / 8.19:
2-Indolylacyl radicals in the synthesis of indole compounds / M.-Lluisa Bennasar ; Tomas Roca8.20:
Radical reactions in synthesis: a short overview
2-Indolylacyl radicals: intermolecular and cascade reactions
Intermolecular addition reactions / 1.3.1:
Intermolecular addition-indole cyclisation cascade reactions / 1.3.2:
Intramolecular reactions of 2-indolylacyl radicals with alkenes
Cyclization of 5-hexenoyl radicals. Total synthesis of ([plus or minus])-guatambuine / 1.4.1:
Cyclization of 6-heptenoyl radicals / 1.4.2:
Cyclization of 7-octenoyl radicals / 1.4.3:
Intramolecular reactions of 2-indolylacyl radicals with aromatic and heteroaromatic systems
Cyclization upon benzenes / 1.5.1:
Cyclization upon pyridines / 1.5.2:
Cyclization upon quinolines. Synthesis of calothrixin B / 1.5.3:
Acknowledgments / 1.6:
Cascade reactions of carbonyl ylides for heterocyclic synthesis / 1.8:
Carbonyl ylide cycloadditions
Intramolecular carbenoid-carbonyl cyclization sequence
Application of the method toward complex tetrahydrofuranyl natural products
Isomunchnone cycloadditions
Intramolecular isomunchnone cycloadditions / 2.2.4:
Cyclization-cycloaddition-cationic [pi]-cyclization reactions / 2.2.5:
Cycloadditions across heteroaromatic [pi]-systems / 2.2.6:
Push-pull carbonyl ylide cycloadditions / 2.2.7:
Azetidines, 3-azetidinones, and diazetines / David J. Lapinsky3.1:
Fused and spirocyclic [beta]-lactams
Oxetanes, dioxetanes, oxetanediones and 2-oxetanones ([beta]-lactones)
Thiophenes and Se/Te analogs
Pyrroles and benzo analogs / Jonathon S. Russel
Intramolecular approaches to pyrroles
Intermolecular approaches to pyrroles
Transformations of heterocycles and carbocycles to pyrroles
Substitutions at pyrrole nitrogen
Substitution at pyrrole carbon
Transformations of pyrroles to other heterocycles / 5.2.3.4:
Pyrrole natural products
Pyrrole materials
Pericyclic transformations
Substitution and C-2/C-3
Carbazoles and azaindoles
Carbazole natural products and ring synthesis
Azaindole ring synthesis / 5.2.7.2:
Natural products isolation and characterization / 5.2.8.1:
Total synthesis: indole core and side-chain modifications / 5.2.8.2:
[beta]-Carbolines and tetrahydro-[beta]-carbolines / 5.2.8.3:
Oxindole and spirooxindole / 5.2.8.4:
Biochemical and medicinal chemistry / 5.2.9:
Synthesis of thiazoles / 5.2.10:
Synthesis of fused thiazoles
Thiazolium-catalyzed reactions
Synthesis of thiazole-containing natural products
Synthesis of isothiazoles / 5.5.2.8:
Isothiazoles as auxiliaries and reagents in organic syntheses
Pharmaceutically interesting isothiazoles
Thiadiazoles and selenodiazoles
1,3-Selenazoles, 1,3-selenadolidines and 1,3-tellurazoles
Pyridine N-oxides and pyridinium salts / Kristina M.K. Kutterer ; Jeremy J. Clemens ; Aimee L. Crombie5.5.6:
Isoquinolines
Reviews and general studies / Amelia Manlove6.2.1:
Pyridazines and benzo derivatives / 6.2.3:
Syntheses / 6.2.3.1:
Applications / 6.2.3.2:
Pyrimidines and benzo derivatives / 6.2.4:
Pyrazines and benzo derivatives / 6.2.4.1:
With O and/or S atoms (2006) / 6.2.5.1:
[1]Benzopyrans and dihydro[1]benzopyrans (chromenes and chromans)
[2]Benzopyrans and dihydro[2]benzopyrans (isochromenes and isochromans)
Tetraoxanes / 6.4.4.3:
With O and/or S atoms (2007)
Pyrylium salts
Benzoazepines and derivatives / Jason A. Smith ; John H. Ryan
Oxepine and fused derivatives
Thiepine and fused derivatives / 7.2.5:
Carbon-nitrogen-sulfur-metal rings
Carbon-phosphous-oxygen-metal rings
Carbon-nitrogen-phosphorus-sulfur-metal rings
Biocatalytic approaches to chiral heterocycles
Ring-expanded ('fat') purines and their nucleoside/nucleotide analogues as broad-spectrum therapeutics
Five-membered ring systems: Thiophenes and Se/Te analogues
Furans and benzofurans With more than one N atom
With O & S (Se, Te) atoms
Pyridine and benzo derivatives
Triazines, tetrazines and fused ring polyaza systems (2007)
Triazines, tetrazines and fused ring polyaza systems (2008)
Recent Advances in the C-2 Regioselective Direct Arylation of Indoles / Tanya C. Boorman ; Igor Larrosa1:
Cross-Coupling Reactions
Direct Arylation Reactions
Oxidative Coupling Reactions
Conclusions
Heterocyclic Dyes: Preparation, Properties, and Applications / S. Shaun Murphree2:
Five-Membered Rings Containing Oxygen: Furanoids
Six-Membered Rings Containing Oxygen: Pyranoids
Five-Membered Rings Containing Nitrogen
Six-Membered Rings Containing Nitrogen
Five-Membered Rings Containing Sulfur / 2.6:
Azetidines, Azetines, and Related Systems / 3:
Monocyclic 2-Azetidinones (β-Lactams)
Fused and Spirocyclic β-Lactams
Oxetanes, Dioxetanes, Dioxetanones and 2-Oxetanones (β-Lactones)
Thietanes, β-Sultams, and Related Systems
Silicon and Phosphorus Heterocycles: Miscellaneous
Five-Membered Ring Systems: Thiophenes and Se/Te Derivatives / Edward R. Biehl5.1:
Reviews, Accounts and Books on Thiophene Chemistry
Synthesis of Thiophenes
Elaboration of Thiophenes and Benzothiophenes
Synthesis of Thiophenes for Use in Material Science
Thiophenes Derivatives in Medicinal Chemistry
Selenophenes and Tellurophenes
Five-Membered Ring Systems: Pyrroles and Benzo Analogs / Jonathan S. Russel ; Sarah J. P. Yoon-Miller5.2:
Synthesis of Pyrroles
Reactions of Pyrroles
Synthesis of Indoles
Reactions of Indoles
Oxindoles and Spirooxindoles
Carbozoles
Azaindoles and Carboline Analogs
Indole Natural Products
Five-Membered Ring Systems: Furans and Benzofurans / Xiao-Shui Peng5.3:
Five Membered Ring Systems: With More than One N Atom / 5.4:
Pyrazoles and Ring-Fused Derivatives
Imidazoles and Ring-Fused Derivatives
1,2,3-Triazoles and Ring-Fused Derivatives
1,2,4- Triazoles and Ring-Fused Derivatives
Tetrazoles and Ring-Fused Derivatives
Five-Membered Ring Systems: With N and S (Se) Atoms / Y.-J. Wu5.5:
Thiadiazoles and Selenodiazoles
Selenazoles, 1,3-Selenadolidines and Telenazoles
Five-Membered Ring Systems: With O & S (Se, Te) Atoms / 5.6:
1,3-Dioxoles and Dioxolanes
1,3-Dithioles and Dithiolanes
1,3-Oxathioles and Oxathiolanes
1,2-Dithioles and Dithiolanes
1,2-Oxathioles and Oxathiolanes
Three Hetero Atoms
Five-Membered Ring Systems with O & N Atoms / 5.7:
Six-Membered Ring Systems: Pyridines and Benzo Derivatives / Philip E. Alford6.1:
Special Topic: Supramolecular Chemistry
Six-Membered Ring Systems: Diazines and Benzo Derivatives / Michael M. Miller ; Albert J. DelMonte6.2:
Pyridazines and Benzo Derivatives
Pyrimidines and Benzo Derivatives
Pyrazines and Benzo Derivatives
Fused [6]+[5] Polyaza Systems / Dmitry N. Kozhevnikov ; Anton M. Prokhorov6.3:
Fused [6]+[6] Polyaza Systems
Six-Membered Ring Systems: With O and/or S Atoms / 6.4:
Heterocycles Containing One Oxygen Atom
Heterocycles Containing One Sulfur Atom
Heterocycles Containing Two or More Oxygen Atoms
Heterocycles Containing Two or More Sulfur Atoms
Heterocycles Containing Both Oxygen and Sulfur in the Same Ring
Seven-Membered Systems Containing One Heteroatom / Peter P. Molesworth ; Christopher J. T. Hyland7:
Seven-Membered Systems Containing Two Heteroatoms
Seven-Membered Systems Containing Three or More Heteroatoms
Seven-Membered Systems of Pharmacological Significance
Future Directions
Carbon-Oxygen Rings / 8:
Carbon-Nitrogen Rings
Carbon-Sulfur Rings
Carbon-Selenium Rings
Carbon-Nitrogen-Oxygen Rings
Carbon-Nitrogen-Sulfur Rings
Carbon-Sulfur-Oxygen Rings
Carbon-Oxygen-Silicon Rings
Carbon-Oxygen-Phosphorus Rings
Carbon-Nitrogen-Phosphorus Rings
Carbon-Nitrogen-Selenium Rings
Carbon-Nitrogen-Sulfur-Oxygen Rings
Carbon-Nitrogen-Phosphorus-Sulfur Rings
Carbon-Nitrogen-Metal Rings
Carbon-Nitrogen-Oxygen-Metal Rings
Carbon-Nitrogen-Sulfur/Phosphorus-Metal Rings
Recent Advances in the Synthesis of Aspidosperma-Jype Alkaloids / Justin M. Lopchuk
Aspidospermine and Aspidospermidine
Aspidofractinine
Tabersonine
Subincanadines
Meloscine
Miscellaneous Approaches to the General Aspidosperma Core
Vindoline, Vinblastine, and Vincristine
Aspidophytine and Haplophytine / 1.9:
Conophylline and Conophyliidine / 1.10:
Synthesis of Heterocycles by Palladium-Catalyzed Intramolecular Heteroarylation / Dmytro Tymoshenko ; Gyorgy Jeges ; Brian T. Gregg
Introduction and Scope of the Review
Annulation of Five-Membered Aza-Rings
Annulation of Six-Membered Aza-Rings
Annulation of Medium Size Aza-Rings
Macrocycles
Tandem Sequences, Cascades, and Miscellaneous Cyclizations
Monocyclic 2-azetidinones (β-lactams) / 2.7:
Fused and Spirocyclic β-lactams
Oxetanes, Dioxetanes, Dioxetanones, and 2-oxetanones (β-lactones)
Thietanes and Related Systems
Reviews, Accounts, and Books on Thiophene, Selenophene, and Tellurophene Chemistry
Synthesis of Thiophenes For Use in Material Science
Thiophene Derivatives in Medicinal Chemistry
Carbazoles / Jessica G. Greger
Carboline Analogs and Azaindoles
Five-Membered Ring Systems: With More than One N Atom / Jie Wu
Pyrazoles and Ring-fused Derivatives
Imidazoles and Ring-fused Derivatives
1,2,3-Triazoles and Ring-fused Derivatives
1,2,4-Triazoles and Ring-fused Derivatives
Tetrazoles and Ring-fused Derivatives
Selenazoles
Five-Membered Ring Systems: With O and S (Se, Te) Atoms
1,3-Dioxoles and 1,3-Dioxolanes
1,3-Dithioles and 1,3-Dithiolanes
1,3-Oxathioles and 1,3-Oxathiolanes
1,2-Dithioles and 1,2-Dithiolanes
1,2-Oxathioles and 1,2-Oxathiolanes
Three Heteroatoms
Five-Membered Ring Systems with O and N Atoms
Triazines, Tetrazines, and Fused Ring Polyaza Systems
Fused [6] + [5] Polyaza Systems
Fused [6] + [6] Polyaza Systems
Six-Membered Ring Systems: With 0 and/or S Atoms
Heterocydes Containing One Oxygen Atom
Heterocydes Containing One Sulfur Atom
Heterocydes Containing Two or More Oxygen Atoms
Heterocydes Containing Two or More Sulfur Atoms
Heterocydes Containing Both Oxygen and Sulfur in the Same Ring
Seven-membered Systems Containing Three or More Heteroatoms / Jarrod L. Green ; Christopher Hyland ; Charlotte C. Williams
Carbon-Silicon Rings
Carbon-Oxygen/Carbon-Nitrogen-Oxygen Rings
Carbon-Sulfur-Phosphorus/Arsenic/Antimony/Bismuth Rings
Carbon-Selenium-Iron Rings
Heterocycles and Medicine: A Survey of the Heterocyclic Drugs Approved by the U.S. FDA from 2000 to Present
Furan and Benzofuran
Thiophene
Pyrrole
Thiazole
Imidazole and Fused Imidazole
Triazole
Pyrazole
Oxadizole and Thiadiazole
Pyridine
Pyrimidine and Pyrimidinone / 1.11:
Pyrazine / 1.12:
Piperazine / 1.13:
Morpholine / 1.14:
Indole / 1.15:
Indazole / 1.16:
Oxindole / 1.17:
Quinoline and Dihydroquinoiine / 1.18:
Benzoazepines and Oxepine / 1.19:
Pyrrolopyrimidine and Pyrrolopyridine / 1.20:
Benzoisoxazoles and Benzoisothiazole / 1.21:
Quinazoline / 1.22:
Quinoxaline / 1.23:
Pteridine / 1.24:
Progress in Quinoxaline Synthesis (Part 1) / Vakhid A. Mamedov ; Nataliya A. Zhukova1.25:
Inttoduaion
Condensation of 1,2-Diaminobenzenes (1,2-DABs; ortho-Phenylenediamines) and Derivatives with Various Two-Carbon Unit Suppliers
Condensation of o-Benzoquinone Diimines and Diimides with Various Two-Carbon Unit Suppliers
Oxetanes, Dioxetanes, and 2-Oxetanones (β-Lactones)
Silicon and Phosphorus Heterocycles. Miscellaneous
Synthesis of Thiophenes, Se/Te for Use in Material Science
Thiophene, Se/Te Derivatives in Medicinal Chemistry
Isatins, Oxindoles, Indoxyls, and Spirooxindoles
Isoindoies
1,2,4-Triazoles and Ring-Fused Derivatives
Thiadiazoles
Five-Membered Ring Systems: With 0 and S (Se, Te) Atoms
Six-Membered Ring Systems: Pyridine and Benzo Derivatives / Tara L.S. Kishbaugh
Synthesis of Pyridine N-Oxides
Reactions of Pyridine N-Oxides
Isoquinolines and Quinolines
Carbon-Phosphorus Rings / Clementina M.M. Santos ; Artur M.S. Silva ; Adam G. Meyer ; JieXiang Yin
Carbon-Oxygen-Sulfur Rings
Carbon-Oxygen/Nitrogen-Phosphorus Rings
Carbon-Sulfur-Arsenic Rings
Carbon-Nitrogen-Oxygen-Sulfur Rings
Carbon-Nitrogen-Oxygen-Phosphorus Rings
Chapter headings: Substituted Heterocyclic Compounds by Selective Control of Halogen-Dance Reactions / J. Frohlich
Heterocycles as Vehicles for Synthesis / A. Padwa
Three-Membered Ring Systems / S.S. Murphree
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