Series - Comprehensive Organic Synthesis II / Organic Synthesis II [2014, PDF, ENG] torrent

Книги и журналы » Точные, естественные и инженерные науки » Химия / Биохимия

Comprehensive Organic Synthesis II / Органический синтез II

Год издания: 2014
Редакторы: Knochel P., Molander G. A. / Кночел П., Моландер Г. А.
Жанр или тематика: Химия
Издательство: Elsevier
ISBN eBook: 9780080977430
ISBN Print: 9780080977423
Язык: Английский
Формат: PDF
Качество: Издательский макет или текст (eBook)
Первое издание: Trost B., Fleming I. - Comprehensive Organic Synthesis / Органический синтез - 1991
Источник: ScienceDirect: Comprehensive Organic Synthesis (Second Edition)

Описание:
Второе издание книги Органический синтез - лауреат премии 2015 PROSE для многотомных научных референтных изданий от Ассоциации американских издателей - опирается на весьма уважаемое первое издание в плане сближения новых общих тем, которые лежат в основе многих разрозненных областей органической химии. Эти темы поддерживают эффективные и действенные стратегии синтеза, тем самым обеспечивая полный обзор этой важной дисциплины.

Полностью пересмотренное и обновленное издание этого многотомника формирует существенный справочный материал для всех тех, кто ищет информацию о решении синтетических проблем, являются ли они опытными практикующими химиками или теми, чьи основные интересы лежат за пределами органического синтеза. Кроме того, химики-синтетики, нуждающиеся в существенных фактах в новых областях, а также студенты совершенные новички в этой области, найдут Comprehensive Organic Synthesis II бесценным источником, который обеспечивает авторитетный обзор основных концепций.

Description:
The second edition of Comprehensive Organic Synthesis—winner of the 2015 PROSE Award for Multivolume Reference/Science from the Association of American Publishers—builds upon the highly respected first edition in drawing together the new common themes that underlie the many disparate areas of organic chemistry. These themes support effective and efficient synthetic strategies, thus providing a comprehensive overview of this important discipline.

Fully revised and updated, this new set forms an essential reference work for all those seeking information on the solution of synthetic problems, whether they are experienced practitioners or chemists whose major interests lie outside organic synthesis. In addition, synthetic chemists requiring the essential facts in new areas, as well as students completely new to the field, will find Comprehensive Organic Synthesis, Second Edition an invaluable source, providing an authoritative overview of core concepts.
[spoiler="Примеры страниц"]

[/spoiler]
[spoiler="Список книг"]
Volume 1: Additions to C–X Π-Bonds, Part 1
Volume 2: Additions to C–X Π-Bonds, Part 2
Volume 3: Carbon–Carbon Bond Formation
Volume 4: Additions to and Substitutions at C–C Π-Bonds
Volume 5: Combining C–C Π-Bonds
Volume 6: Heteroatom Manipulation
Volume 7: Oxidation
Volume 8: Reduction
Volume 9: Enabling Technologies for Organic Synthesis
[/spoiler]
[spoiler="Оглавление"]
Volume 1: Additions to C–X Π-Bonds, Part 1
Introduction to Volume 1: Additions to Csingle bondX π-Bonds, Part 1, Page xxv
1.01 Carbanions of Alkali and Alkaline-Earth Cations: (II) Selectivity of Carbonyl Addition Reactions, Pages 1-26, D.M. Huryn
1.02 Organosilicon Reagents: Vinyl-, Alkynyl-, and Arylsilanes, Pages 27-48, P. Somfai, B. Seashore-Ludlow
1.03 Organoaluminum Reagents, Pages 49-73, K. Maruoka, Y. Naganawa
1.04 Regio-, Diastereo-, and Enantioselective Addition of Organocopper Reagents onto Cdouble bond; length as m-dashO and Cdouble bond; length as m-dashN Bonds, Pages 74-123, E. Vrancken, J.-M. Campagne, P. Mangeney
1.05 Organotitanium and Organozirconium Reagents, Pages 124-158, O. Kulinkovich
1.06 Organochromium Reagents, Pages 159-203, K. Takai
1.07 Recent Advances in Organozinc Reagents, Pages 204-266, T. Hirose, K. Kodama
1.08 Organocerium Reagents, Pages 267-277, E. Marcantoni, L. Sambri
1.09 Samarium and Ytterbium Reagents, Pages 278-343, K.A. Choquette, R.A. Flowers II
1.10 Lewis Acid Promoted Addition Reactions of Organometallic Compounds, Pages 344-364, E. Marcantoni, M. Petrini
1.11 Nucleophilic Addition of Nonstabilized Carbanions to Imines and Imine Derivatives, Pages 365-394, V.N.G. Lindsay, A.B. Charette
1.12 Sulfur and Selenium Stabilization, Pages 395-423, C. Ni, J. Hu
1.13 Benzoin and Aza-benzoin, Pages 424-470, X. Bugaut
1.14 Oxygen-Stabilized Carbanions, Pages 471-515, S. Florio, F.M. Perna, A. Salomone, P. Vitale
1.15 Olefination of Carbonyl Compounds by Main-Group Element Mediators, Pages 516-608, P.R. Blakemore
1.16 Epoxidation and Related Processes, Pages 609-652, J.B. Sweeney, A.E.J. Walsh
1.17 Addition of Heteroatom Nucleophiles to Cdouble bond; length as m-dashO and Cdouble bond; length as m-dashN pi Bonds, Pages 653-696, Z. Zhang, M.J. Kaplan, J.C. Antilla
1.18 CN Addition to Cdouble bond; length as m-dashO and Cdouble bond; length as m-dashN Bonds, Pages 697-750, P. Merino
1.19 Carbonyl and Imine Activation, Pages 751-769, H. Miyabe, Y. Takemoto

Volume 2: Additions to C–X Π-Bonds, Part 2
Introduction to Volume 2: Additions to Csingle bondX π-Bonds, Part 2, Page xiii
2.01 Allylborons, Pages 1-71, P.V. Ramachandran, P.D. Gagare, D.R. Nicponski
2.02 Allylsilanes, Allylstannanes, and Related Compounds, Pages 72-147, P.V. Ramachandran, D.R. Nicponski, P.D. Gagare
2.03 Prins Reactions and Carbonyl, Imine, and Thiocarbonyl Ene Reactions, Pages 148-191, B.B Snider
2.04 Heteroatom-Stabilized Allylic Anions, Pages 192-208, H. Yorimitsu, K. Oshima
2.05 Propargyl and Allenyl Organometallics, Pages 209-242, H. Yamamoto, D.L. Usanov
2.06 Formation of Enolates, Pages 243-272, H.B. Mekelburger, C.S. Wilcox
2.07 The Aldol Reaction: Organocatalysis Approach, Pages 273-339, N. Mase, Y. Hayashi
2.08 The Aldol Reaction: Group I and Group II Enolates, Pages 340-395, C.H. Heathcock
2.09 The Aldol Reaction: Group IV Enolates (Mukaiyama, Enol Ethers), Pages 396-450, S. Kobayashi, Y. Yamashita, W.-J. Yoo, T. Kitanosono, J.-F. Soulé
2.10 The Aldol Reaction: Transition Metal Enolate, Pages 451-511, T. Harada, A. Abiko
2.11 Aldolase-Catalyzed Csingle bondC Bond Formation of Carbohydrate Synthesis, Pages 512-522, T. Sugai, K. Fuhshuku
2.12 Zinc Enolates: The Reformatsky and Blaise Reactions, Pages 523-542, A. Baba, M. Yasuda, Y. Nishimoto
2.13 The Henry (Nitroaldol) Reaction, Pages 543-570, H. Sasai
2.14 Other Condensation Reactions (Knoevenagel, Perkin, Darzens), Pages 571-605, K. Ebitani
2.15 Metal Homoenolates, Pages 606-628, M. Kimura
2.16 The Bimolecular and Intramolecular Mannich and Related Reactions, Pages 629-681, T. Akiyama
2.17 Addition to N-Acyliminium Ions of Heteroatoms such as Oxygen, Nitrogen, Sulfur, and Selenium as Internal Nucleophiles, Pages 682-742, A. Daïch, A. Ghinet, B. Rigo

Volume 3: Carbon–Carbon Bond Formation
Introduction to Volume 3: Carbonsingle bondCarbon Bond Formation, Page xiii
3.01 Alkylations of Enols and Enolates, Pages 1-55, B.M. Stoltz, N.B. Bennett, D.C. Duquette, A.F.G. Goldberg, Y. Liu, M.B. Loewinger, C.M. Reeves
3.02 Organolithium Compounds Bearing a Phenyl-, a Vinyl-, and/or a Seleno Group on their Carbanionic Centers: Synthesis by Se/Li Exchange and Unusual Synthetic Applications, Pages 56-156, A. Krief, A. Kremer
3.03 Alkylation of α-Sulfur-Containing Carbanions, Pages 157-208, R. Fernández de la Pradilla, A. Viso
3.04 Alkylations of Nonstabilized Carbanions, Pages 209-267, A. Mordini, G. Reginato, L. Zani
3.05 Polyene Cyclizations, Pages 268-292, S.A. Snyder, A.M. Levinson
3.06 Transannular Electrophilic Cyclizations, Pages 293-336, T.T.H. Dao, T. Marmin, Y.L. Dory
3.07 Coupling Reactions Between sp3-Carbon Centers, Pages 337-391, T. Iwasaki, N. Kambe
3.08 Coupling Reactions Between sp3 and sp2 Carbon Centers, Pages 392-464, G. Manolikakes
3.09 Coupling Reactions Between C(sp2) and C(sp) Carbon Centers, Pages 465-527, D. Gelman, I. Shaposhnikov
3.10 Coupling Reactions Between sp Carbon Centers, Pages 528-579, M. Alami, A. Hamze, S. Messaoudi
3.11 Pinacol Coupling Reactions, Pages 580-620, K. Suzuki, M. Tamiya
3.12 Acyloin Coupling Reactions, Pages 621-655, K.A. Scheidt, E.A. O'Bryan
3.13 Oxidative Coupling of Phenols and Phenol Ethers, Pages 656-740, S. Quideau, D. Deffieux, L. Pouységu
3.14 The Pinacol Rearrangement, Pages 741-756, M.K. Muñiz
3.15 Acid-Catalyzed Rearrangement of Epoxides, Pages 757-794, M. Gouygou, M. Urrutigoïty
3.16 The Semipinacol Rearrangements, Pages 795-852, S.-H. Wang, Y.-Q. Tu, M. Tang
3.17 The Favorskii Rearrangement (Extend to Rings), Pages 853-886, E. Butkus
3.18 The Ramberg–Bäcklund Rearrangement and the Eschenmoser Coupling Reaction, Pages 887-943, S. Braverman, M. Cherkinsky
3.19 The Wolff Rearrangement, Pages 944-991, N.R. Candeias, A.F. Trindade, P.M.P. Gois, C.A.M. Afonso
3.20 Nitrogen- and Sulfur-Based Stevens and Related Rearrangements, Pages 992-1037, R. Bach, S. Harthong, J. Lacour
3.21 The Wittig Rearrangement, Pages 1038-1072, J.P. Wolfe
3.22 Carbonylation and Decarbonylation Reactions, Pages 1073-1100, T. Fukuyama, S. Maetani, I. Ryu
3.23 Carbon–Carbon σ-Bond Formation via Csingle bondH Bond Functionalization, Pages 1101-1209, Y.-H. Zhang, G.-F. Shi, J.-Q. Yu

Volume 4: Additions to and Substitutions at C–C Π-Bonds
Introduction to Volume 4: Additions to and Substitutions at C–C π-Bonds, Pages xiii-xiv
4.01 Stabilized Nucleophiles with Electron Deficient Alkenes, Alkynes, Allenes, Pages 1-85, W.-Q. Chen, J.-A. Ma
4.02 Nucleophilic Addition-Electrophilic Coupling with a Carbanion Intermediate, Pages 86-118, X. Song, W. Wang
4.03 Organocatalytic Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes, Pages 119-188, J.L. Vicario, E. Reyes, L. Carrillo, U. Uria
4.04 Metal-Catalyzed Asymmetric Nucleophilic Addition to Electron-Deficient Alkenes, Pages 189-341, M. Mauduit, O. Baslé, H. Clavier, C. Crévisy, A. Denicourt-Nowicki
4.05 Addition of Hsingle bondX Reagents to Alkenes, Alkynes, and Allenes without Transition Metal, Pages 342-391, W. Li, J. Zhang
4.06 Addition of X–Y Reagents to Alkenes, Alkynes, and Allenes, Pages 392-411, A. Ogawa
4.07 Electrophilic Cyclization, Pages 412-494, X. Jiang, H. Liu
4.08 Carbon–Carbon Bond-Forming Reactions Involving Aryl Radicals, Pages 495-516, S.G. Hammer, M.R. Heinrich
4.09 Nucleophilic Coupling with Arynes, Pages 517-579, H. Yoshida
4.10 Reactions of Nucleophiles with Coordinated Alkynes, Alkenes, and Allenes, Pages 580-647, W. Bai, J. Chen, G. Jia
4.11 Nucleophiles with Allyl Metal Complexes, Pages 648-698, C.-H. Ding, X.-L. Hou
4.12 Radical Addition Reactions, Pages 699-741, H. Subramanian, Y. Landais, M.P. Sibi
4.13 Radical Cyclizations and Sequential Radical Reactions, Pages 742-809, B.M. Loertscher, S.L. Castle
4.14 Vinyl Substitutions with Organopalladium Intermediates, Pages 810-890, E.M. Butler, R. Doran, C.M. Wilson, P.J. Guiry
4.15 Carbometalation and Heterometalation Reactions of Alkenes, Alkynes, and Allenes, Pages 891-938, A. Ding, H. Guo
4.16 Bismetallation and Bismetallative Reaction of Alkenes, Alkynes, and Allenes, Pages 939-960, J.P. Morken
4.17 Hydroacylation of Alkenes, Alkynes, and Allenes, Pages 961-994, M.C. Willis
4.18 Hydroformylation and Related Carbonylation Reactions of Alkenes, Alkynes, and Allenes, Pages 995-1053, B. Breit, L. Diab
4.19 Methylene and Nonfunctionalized Alkylidene Transfer to Form Cyclopropanes, Pages 1054-1080, A.B. Charette
4.20 Addition of Ketocarbenes to Alkenes, Alkynes, and Aromatic Systems, Pages 1081-1280, J.I. García, L. Salvatella, E. Pires, J.M. Fraile, J.A. Mayoral
4.21 Intramolecular 1,3‐Dipolar Cycloadditions of Alkenes, Alkynes, and Allenes, Pages 1281-1341, R.S. Menon, V. Nair
4.22 Intermolecular 1,3-Dipolar Cycloadditions of Alkenes, Alkynes, and Allenes, Pages 1342-1383, L.-J. Wang, Y. Tang
4.23 Stetter Reaction, Pages 1384-1406, M. Gravel, J.M. Holmes

Volume 5: Combining C–C Π-Bonds
Introduction to Volume 5: Combining C–C π-Bonds, Pages xiii-xiv
5.01 Ene Reactions with Carbon Enophiles – Metallo-Ene Reactions, Pages 1-65, T.J.J. Müller
5.02 Thermal Cyclobutane Ring Formation, Pages 66-84, B. Alcaide, C. Aragoncillo, P. Almendros
5.03 Formation of Four-Membered Heterocycles, Pages 85-128, R. Robiette, J. Marchand-Brynaert
5.04 Photochemical Cycloadditions, Pages 129-158, A.G. Griesbeck, M. Franke
5.05 The Paternò–Büchi Reaction, Pages 159-199, M. D'Auria
5.06 Di-π-methane, Oxa-di-π-methane, and Aza-di-π-methane Photoisomerization, Pages 200-221, E. Riguet, N. Hoffmann
5.07 Metal-Mediated and Metal-Catalyzed [2+2] Cycloadditions, Pages 222-272, K. Parthasarathy, C.-H. Cheng
5.08 Thermal and Metal-Induced [3+2] Cycloadditions, Pages 273-350, N. Iwasawa
5.09 Intermolecular Diels–Alder Reactions, Pages 351-408, K. Ishihara, A. Sakakura
5.10 Hetero-Diels–Alder Reactions, Pages 409-465, K. Ishihara, A. Sakakura
5.11 Intramolecular and Transannular Diels–Alder Reactions, Pages 466-517, D. Tanner, E. Ascic
5.12 Retro Diels–Alder Reactions, Pages 518-594, F. Csende, G. Stájer, F. Fülöp
5.13 (4+3) Cycloadditions, Pages 595-655, J.L. Mascareñas, M. Gulías, F. López
5.14 Higher Order Cycloadditions, Pages 656-702, P.A. Inglesby, P.A. Evans
5.15 The Arene–Alkene Photocycloaddition, Pages 703-731, T. Gaich
5.16 Cyclobutene Ring Opening Reactions, Pages 732-782, M. Murakami, T. Matsuda
5.17 1,3-Cyclohexadiene Formation Reactions: 6π and Higher-Order Electrocyclizations, Pages 783-826, D. Trauner, R. Webster
5.18 The Nazarov Cyclization, Pages 827-866, F.G. West, O. Scadeng, Y-K Wu, R.J. Fradette, S. Joy
5.19 Cope, Oxy-Cope, and Anionic Oxy-Cope Rearrangements, Pages 867-911, C. Schneider, C.F. Weise
5.20 Claisen Rearrangements, Pages 912-977, A.M. Martín-Castro, M. Tortosa
5.21 Consecutive Sigmatropic Rearrangements, Pages 978-998, L. Barriault, B. Sow, M.S. Sherburn
5.22 Rearrangements of Vinylcyclopropanes, Divinylcyclopropanes, and Related Systems, Pages 999-1076, S. Vshyvenko, J.W. Reed, T. Hudlicky, E. Piers
5.23 Anion- and Metal-Promoted Rearrangements of Small-Ring Systems, Pages 1077-1105, N. Cramer
5.24 The Pauson–Khand Reaction, Pages 1106-1178, N. Jeong
5.25 Metal Carbene Cycloadditions, Pages 1179-1256, J.W. Herndon
5.26 Cross Metathesis, Pages 1257-1301, K. Żukowska, K. Grela
5.27 Ene–Yne Metathesis, Pages 1302-1356, S.T. Diver, J.R. Clark
5.28 Alkyne Metathesis, Pages 1357-1399, A. Fürstner
5.29 Ring-Closing Metathesis, Pages 1400-1482, B. Schmidt, S. Hauke, S. Krehl, O. Kunz
5.30 Noble Metal-Catalyzed Enyne Cycloisomerizations and Related Reactions, Pages 1483-1536, V. Michelet
5.31 [2+2+2] Cycloadditions, Pages 1537-1581, G Domínguez, J Pérez-Castells
5.32 Hydrovinylation Reactions in Organic Synthesis, Pages 1582-1620, T.V. RajanBabu, G. Adam Cox, H.J. Lim, N. Nomura, R.K. Sharma, C.R. Smith, A. Zhang
5.33 Hydroarylation Reactions, Pages 1621-1659, T de Haro, C Nevado
5.34 Early Transition Metal Mediated Reductive Coupling Reactions, Pages 1660-1737, G.C. Micalizio
5.35 Transition-Metal-Catalyzed Cycloaddition of Small Ring Compounds, Pages 1738-1771, C. Aïssa
5.36 Hydrocyanation in Organic Synthesis, Pages 1772-1793, T.V. RajanBabu

Volume 6: Heteroatom Manipulation
Introduction to Volume 6: Heteroatom Manipulation, Pages xiii-xv
6.01 Synthesis of Glycosides, Pages 1-33, L. Bohé, D. Crich
6.02 Synthesis of Amines and Ammonium Salts, Pages 34-99, C.C. Marvin
6.03 Synthesis of Nitroso, Nitro, and Related Compounds, Pages 100-130, N. Nishiwaki
6.04 Synthesis of Sulfides, Sulfoxides, and Sulfones, Pages 131-174, J. Drabowicz, P. Kiełbasiński, A. Zając, P. Wach-Panfiłow
6.05 Synthesis of Phosphonium Ylides, Pages 175-209, I.L. Odinets, D.V. Aleksanyan
6.06 Synthesis of Fluorides, Pages 210-238, T. Liang, T. Ritter
6.07 Ritter-Type Reactions, Pages 239-295, R. Bishop
6.08 Acylation-Type Reactions: Synthesis of Esters via Acyl Transfer, Pages 296-354, D. Zell, P.R. Schreiner
6.09 Synthesis of Esters and Lactones, Pages 355-410, P. Siengalewicz, J. Mulzer, U. Rinner
6.10 Synthesis of Thioamides and Thiolactams, Pages 411-426, E. Schaumann
6.11 N-Acylation Reactions of Amines, Pages 427-478, J.E. Taylor, S.D. Bull
6.12 Inorganic Acid Derivatives, Pages 479-554, P.R. Hanson, N. Asad, Q. Zang, S. Jayashinghe, J. Markley
6.13 Use of Carbonyl Derivatives for Heterocyclic Synthesis, Pages 555-572, G.E. Schiltz
6.14 Functional Group Transformations via Carbonyl Derivatives, Pages 573-597, M. Uyanik, K. Ishihara
6.15 Hofmann, Curtius, Schmidt, Lossen, and Related Reactions, Pages 598-635, J. Aubé, C. Fehl, R. Liu, M.C. McLeod, H.F. Motiwala
6.16 Functional Group Transformation via Allyl Rearrangement, Pages 636-754, Z. Gu, A. Zakarian
6.17 Polonovski- and Pummerer-type Reactions and the Nef Reaction, Pages 755-801, S.K. Bur
6.18 Eliminations to Form Alkenes, Allenes, and Alkynes and Related Reactions, Pages 802-841, R.A. Biggs, W.W. Ogilvie
6.19 Fragmentation Reactions, Pages 842-860, T.T. Hoang, G.B. Dudley, L.J. Williams

Volume 7: Oxidation
Introduction to Volume 7: Oxidation, Pages xiii-xiv
7.01 Oxidation by Dehydrogenation, Pages 1-25, S.F. Kirsch, M. Wegener
7.02 Oxidation by Metals (Nitrene), Pages 26-85, C.-M. Che, V.K.-Y. Lo, C.-Y. Zhou
7.03 Asymmetric C–H Functionalization by Transition Metal-Catalyzed Carbene Transfer Reactions, Pages 86-120, X.P. Zhang, X. Cui
7.04 Oxidation by Microbial Methods, Pages 121-144, R. Wohlgemuth
7.05 Oxidation Adjacent to Cdouble bond; length as m-dashC Bonds, Pages 145-177, K.J. Fraunhoffer
7.06 Oxidation Adjacent to Cdouble bond; length as m-dashX Bonds by Dehydrogenation, Pages 178-212, S.S. Stahl, T. Diao
7.07 α-Oxygenation of Carbonyl Compounds, Pages 213-241, M.J. Bouma, B. Olofsson
7.08 Oxidation Adjacent to Nitrogen, Pages 242-261, X.-J. Dai, C.-J. Li
7.09 Oxidation of C–H Bond Adjacent to Oxygen of Ethers, Pages 262-276, Y. Obora, Y. Ishii
7.10 Oxidation Adjacent to Oxygen of Alcohols by Chromium Reagents, Pages 277-294, S. Chandrasekaran, V. Ganesh
7.11 Oxidation Adjacent to Oxygen of Alcohols Catalyzed by Palladium/Dimethyl Sulfoxide, Pages 295-301, J. Muzart
7.12 Directed Aryl C–H Oxidations with Main Group Metals, Pages 302-312, B.-T. Guan, Z.-J. Shi
7.13 Directed Aryl Csingle bondH Oxidations with Transition Metals, Pages 313-346, A. Lei, W. Liu
7.14 Nondirected Aryl C–H Oxidations, Pages 347-372, M.R. Smith III, B. Chattopadhyay
7.15 Synthesis of para- and ortho-Quinones, Pages 373-410, M.G. Weaver, T.R.R. Pettus
7.16 Addition Reactions with Formation of Carbon-Heteroatom Bonds: (III) Asymmetric Methods of Dihydroxylation, Aminohydroxylation, and Diamination, Pages 411-430, K. Muñiz
7.17 Addition Reactions with Formation of Carbon–Oxygen Bonds: (iv) The Wacker Oxidation and Related Reactions, Pages 431-491, K. Takenaka, H. Sasai
7.18 Addition Reactions with Formation of Carbon–Carbon Bonds: (v) The Oxidative Heck Reaction, Pages 492-537, L.R. Odell, J. Sävmarker, J. Lindh, P. Nilsson, M. Larhed
7.19 Addition Reactions with Formation of Carbonsingle bondNitrogen Bonds, Pages 538-604, P. Dauban, B. Darses, A. Jarvis
7.20 Addition Reactions with Formation of Carbon–Sulfur and Carbon Selenium Bonds, Pages 605-637, C. Santi, C. Tidei
7.21 Addition Reactions with Formation of Carbonsingle bondHalogen Bonds, Pages 638-691, U. Hennecke, C. Rösner, T. Wald, T. Robert, M. Oestreich
7.22 Oxidation of Carbon–Boron Bonds, Pages 692-718, T. Chinnusamy, K. Feeney, C.G. Watson, D. Leonori, V.K. Aggarwal
7.23 Oxidation of Carbon–Metal Bonds, Pages 719-743, D.C. Powers, T. Ritter
7.24 Oxidation of Carbon–Halogen Bonds, Pages 744-769, A. Itoh, T. Miura, N. Tada
7.25 The Beckmann and Related Reactions, Pages 770-800, S. Chandrasekhar
7.26 Glycol Cleavage Reactions, Pages 801-817, A.W.H. Wong, T.K.M. Shing
7.27 The Hunsdiecker and Related Reactions, Pages 818-836, D. Crich, K. Sasaki
7.28 Oxidation of Sulfur, Selenium, and Tellurium, Pages 837-879, A. Lattanzi
7.29 Oxidative Functionalization with Hypervalent Halides, Pages 880-933, F.V. Singh, T Wirth

Volume 8: Reduction
Introduction to Volume 8: Reduction, Page xiii
8.01 Reduction of C=O to CHOH by Metal Hydrides, Pages 1-84, A.F. Abdel-Magid
8.02 Reduction of Cdouble bond; length as m-dashN to CH–NH by Metal Hydrides, Pages 85-150, A.F. Abdel-Magid
8.03 Reduction of Cdouble bond; length as m-dashN to CHNH by Hydride Delivery from C, Pages 151-197, E. Arceo, P. Melchiorre
8.04 Reduction of Cdouble bond; length as m-dashO to CHOH by Metal-Catalyzed Hydrogenation and Transfer Hydrogenation, Pages 198-273, X. Wu, J. Xiao
8.05 Reduction of Cdouble bond; length as m-dashN to CHNH by Metal-Catalyzed Hydrogenation and Transfer Hydrogenation, Pages 274-299, H.-U. Blaser, F. Spindler
8.06 Reduction of Cdouble bond; length as m-dashX to CHsingle bondXH by Dissolving Metals and Related Methods, Pages 300-316, U. Wille
8.07 Reduction of Cdouble bond; length as m-dashO to CHOH Using Enzymes and Microorganisms, Pages 317-327, M. Truppo
8.08 A Reduction of Cdouble bond; length as m-dashN to CH–NH Using Enzymes and Microorganisms, Pages 328-338, N.J. Turner
8.09 Reduction of O,O-, N,O-, and S,O-Acetals to Ethers, Pages 339-367, E.A. Anderson, C.D. Campbell
8.10 Reduction of Carboxylic Acids and their Derivatives to Alcohols, Ethers, and Amines, Pages 368-409, G.E. Arnott
8.11 Reduction of Carboxylic Acids and their Derivatives to Aldehydes, Pages 410-445, G.E Arnott
8.12 Reduction of Cdouble bond; length as m-dashX to CH2, Pages 446-478, J.W. Burton
8.13 Recent Developments in the Reduction of Nitro and Nitroso Compounds, Pages 479-492, D.J. Dixon, O. Pando Morejón
8.14 Reduction of Ndouble bond; length as m-dashN, N–N, N–O, and O–O Bonds, Pages 493-534, C Kouklovsky, G Vincent
8.15 Reduction of Sdouble bond; length as m-dashO and SO2 to S, S–X to S–H, and Pdouble bond; length as m-dashO to P, Pages 535-563, A.-C. Gaumont, M. Gulea, S. Perrio, V. Reboul
8.16 Heterogeneous Hydrogenation of Cdouble bond; length as m-dashC and Ctriple bond; length of mdashC Bonds, Pages 564-604, S.P. Thomas, M.D. Greenhalgh
8.17 Homogeneous Catalytic Hydrogenation of CåC and CåC, Pages 605-631, D. Ager
8.18 Reduction of CåC and CåC by Noncatalytic Chemical Methods, Pages 632-638, DR Carbery
8.19 Partial Reduction of Benzenoid Aromatic Rings by Dissolving Metals and by Other Methods, Pages 639-672, M.C. Elliott, N.L. Hewitt
8.20 Partial Reduction of Enones, Styrenes, and Related Systems, Pages 673-740, A. Baba, M. Yasuda, Y. Nishimoto
8.21 Partial and Complete Reduction of Pyridine and their Benzo Analogs, Pages 741-793, V. Ratovelomanana-Vidal, P. Phansavath, T. Ayad, M.R. Vitale
8.22 Partial and Complete Reduction of Pyrroles, Furans, Thiophenes, and their Benzo Analogs, Heterocycles Containing More Than One Heteroatom, Pages 794-837, T.J. Donohoe, C.R. Jones, C. Winter
8.23 Hydrozirconation of Alkenes and Alkynes, Pages 838-876, Z. Song, T. Takahashi
8.24 Hydrometallation of Cdouble bond; length as m-dashC and Ctriple bond; length of mdashC Bonds. Group 3, Pages 877-963, M. Zaidlewicz, A. Wolan, M. Budny
8.25 Hydrometallation Group 4 (Si, Sn, Ge, and Pb), Pages 964-998, A.P. Dobbs, F.K.I. Chio
8.26 Reduction of Saturated Alkyl Halides to Alkanes, Pages 999-1010, V.E. Ziffle, S.P. Fletcher
8.27 Reduction of Saturated Alcohols and Amines to Alkanes, Pages 1011-1030, L. Chenneberg, J.-P. Goddard, L. Fensterbank
8.28 Reduction of Sulfursingle bondCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon, Pages 1031-1085, J.M. Manthorpe, H.I. Kong, J.W. Palko, M.A. Gill
8.29 Reduction of Epoxides, Pages 1086-1122, S. Florio, F.M Perna, A. Salomone, P. Vitale
8.30 Reduction of Alkenyl Halides to Alkenes, and of Aryl Halides and Related Compounds to Arenes, Pages 1123-1142, J.D. Nguyen, E.M. D'Amato, C.R.J. Stephenson
8.31 Reduction of Ketones to Alkenes, Pages 1143-1163, A.J. Clark, C.S. Guy
8.32 Hydrogenolysis of Allyl and Benzyl Halides and Related Compounds, Pages 1164-1184, A.J. Bissette, S.P. Fletcher

Volume 9: Enabling Technologies for Organic Synthesis
Introduction to Volume 9: Enabling Technologies for Organic Synthesis, Pages xiii-xv
9.01 Enabling Technologies in High Throughput Chemistry, Pages 1-27, J. Aubé, S.A. Rogers, C. Santini
9.02 High-Throughput Analysis for High-Throughput Experimentation in Organic Chemistry, Pages 28-53, W. Schafer, X. Bu, X. Gong, L.A Joyce, C.J. Welch
9.03 Organic Synthesis in Small Scale Continuous Flow: Flow Chemistry, Pages 54-93, S. Born, E. O'Neal, K.F. Jensen
9.04 Microcapillary Catalysis, Pages 94-110, O. Trapp
9.05 Technology-Enabled Synthesis of Carbohydrates, Pages 111-142, N.L. Snyder, P.H. Seeberger, G.T. Mukosera, E.M.K. Held
9.06 The Use of Preparative Chiral Chromatography for Accessing Enantiopurity in Pharmaceutical Discovery and Development, Pages 143-159, C.J. Welch
9.07 High-Throughput Purification in Support of Pharmaceutical Discovery, Pages 160-180, R. McClain, E. Streckfuss
9.08 Use of Industrial Scale Chromatography in Pharmaceutical Manufacturing, Pages 181-206, O. Dapremont
9.09 High-Throughput Screening to Enable Salt and Polymorph Screening, Chemical Purification, and Chiral Resolution, Pages 207-233, N. Variankaval, M. McNevin, S. Shultz, S. Trzaska
9.10 Organic Synthesis Using Microwave Heating, Pages 234-286, N.E. Leadbeater
9.11 Useful Chemical Activation Alternatives in Solvent-Free Organic Reactions, Pages 287-314, J.G. Hernández, C.G. Avila-Ortiz, E. Juaristi
9.12 Fluorous Linker-Enabled Organic Synthesis, Pages 315-329, W. Zhang
9.13 Organic Photochemistry, Pages 330-350, C.G. Bochet
9.14 Preparative Electrochemistry for Organic Synthesis, Pages 351-389, G.G. Botte, D.A. Daramola, M. Muthuvel
9.15 Synthetic Biology Approaches for Organic Synthesis, Pages 390-420, P.S. Coelho, F.H. Arnold, J.C. Lewis
9.16 Enzyme Evolution as a Tool for Creating Improved Catalysts for Large-Scale Organic Synthesis, Pages 421-437, G.W. Huisman
9.17 Chemistry of Antibody–Small Molecule Drug Conjugates, Pages 438-462, R.M. Garbaccio
9.18 Post-Synthetic Chemical Functionalization of Oligonucleotides, Pages 463-493, Yu Yuan, Weimin Wang
[/spoiler]