Drayton / Backes / Bellus Index Volume Category 4

1. Auflage 2013
ISBN: 978-3-13-178551-0
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 1288 Seiten, PDF, Format (B × H): 170 mm x 255 mm

Reihe: Science of Synthesis

Science of Synthesis provides a critical review of the synthetic methodology developed from the early 1800s to date for the entire field of organic and organometallic chemistry. As the only resource providing full-text descriptions of organic transformations and synthetic methods as well as experimental procedures, Science of Synthesis is therefore a unique chemical information tool. Over 1000 world-renowned experts have chosen the most important molecular transformations for a class of organic compounds and elaborated on their scope and limitations. The systematic, logical and consistent organization of the synthetic methods for each functional group enables users to quickly find out which methods are useful for a particular synthesis and which are not. Effective and practical experimental procedures can be implemented quickly and easily in the lab.// The content of this e-book was originally published in December 2008.

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Bellus, D.

Noyori, R.

Regitz, M.

Schaumann, E.

Shinkai, I.

Drayton, Colin J.

Backes, Jutta

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

1;Science of Synthesis: Category 4 Cumulative Index – Compounds with Two Carbon–Heteroatom Bonds;1
1.1;Imprint;5
1.2;Title page;6
1.3;List of All Volumes;7
1.4;Preface;12
1.5;Table of Contents;14
1.6;Product Class Overview;16
1.7;Structure Index;40
1.7.1;Aldehydes, Ketones, and Derivatives: Monocyclic Compounds;40
1.7.2;Aldehydes, Ketones, and Derivatives: Bicyclic Compounds;83
1.7.3;Aldehydes, Ketones, and Derivatives: Tricyclic Compounds;123
1.7.4;Aldehydes, Ketones, and Derivatives: Tetracyclic Compounds;160
1.7.5;Aldehydes, Ketones, and Derivatives: Pentacyclic Compounds;180
1.7.6;Aldehydes, Ketones, and Derivatives: Hexacyclic Compounds;191
1.7.7;Aldehydes, Ketones, and Derivatives: Heptacyclic Compounds;194
1.7.8;Aldehydes, Ketones, and Derivatives: Octacyclic Compounds;198
1.7.9;Aldehydes, Ketones, and Derivatives: Nonacyclic and Higher Compounds;199
1.8;Name Reaction Index;202
1.8.1;A;202
1.8.2;B;202
1.8.3;C;203
1.8.4;D;204
1.8.5;E;205
1.8.6;F;205
1.8.7;G;206
1.8.8;H;207
1.8.9;I;208
1.8.10;J;208
1.8.11;K;208
1.8.12;L;209
1.8.13;M;209
1.8.14;N;211
1.8.15;O;211
1.8.16;P;211
1.8.17;R;212
1.8.18;S;213
1.8.19;T;214
1.8.20;U;214
1.8.21;V;215
1.8.22;W;215
1.8.23;Y;216
1.8.24;Z;216
1.9;Keyword Index;218
1.9.1;A;218
1.9.2;B;345
1.9.3;C;396
1.9.4;D;422
1.9.5;E;467
1.9.6;F;497
1.9.7;G;502
1.9.8;H;511
1.9.9;I;525
1.9.10;J;537
1.9.11;K;537
1.9.12;L;562
1.9.13;M;564
1.9.14;N;573
1.9.15;O;590
1.9.16;P;601
1.9.17;Q;667
1.9.18;R;670
1.9.19;S;671
1.9.20;T;709
1.9.21;U;731
1.9.22;V;732
1.9.23;W;734
1.9.24;X;735
1.9.25;Y;735
1.9.26;Z;736
1.10;Author Index;738
1.10.1;A;738
1.10.2;B;756
1.10.3;C;797
1.10.4;D;828
1.10.5;E;851
1.10.6;F;859
1.10.7;G;878
1.10.8;H;902
1.10.9;I;935
1.10.10;J;944
1.10.11;K;953
1.10.12;L;993
1.10.13;M;1019
1.10.14;N;1065
1.10.15;O;1081
1.10.16;P;1094
1.10.17;Q;1119
1.10.18;R;1120
1.10.19;S;1144
1.10.20;T;1202
1.10.21;U;1228
1.10.22;V;1231
1.10.23;W;1243
1.10.24;X;1264
1.10.25;Y;1265
1.10.26;Z;1276
1.11;Abbreviations;1286
1.12;List of All Volumes;1292

Leseproben

Name Reaction Index

A

Achmatowicz reaction

– Achmatowicz reaction 29-372

– Achmatowicz ring expansion 29-457

Adams reaction

– Adams modification 31a-441

Alder -principle

– Alder -principle 33-630

aldol reaction

– aldol addition 31a-450, 32-540, 547, 577, 578, 579

– aldol adduct 28-540

– aldol condensation 25-361, 391, 747f., 28-462, 889, 31a-364, 455, 32-156, 547, 33-131

– aldol cyclization 28-481, 31a-366

– aldol products 29-155, 32-565

– aldol reaction 25-721, 29-45, 648, 31a-362, 454f., 31b-1760, 1858, 32-547

– aldolization reaction 31a-365

– aldolization 32-300

– aldol-type condensation 33-15, 52, 131

– aldol-type reaction 25-717, 26-481

– aldol-type reaction, intramolecular 26-184

– cross-aldol condensation 25-747

– cross aldolization 25-748

– nitro-aldol reaction 33-345f., 351

– nitroso aldol reaction 31b-1759

– retro-aldol reaction 29-523

Andersen reaction

– Andersen procedure, modifications 31a-935

– Andersen's sulfoxide synthesis 31a-894

– Andersen-type synthesis 31a-930

– Andersen reaction 33-75

Anelli oxidation

– Anelli oxidation 25-547

– Anelli's protocol 25-547

Apple–Lee reagent

– Apple–Lee reagent 29-908

Arbuzov reaction

– Arbuzov fission 33-746, 747, 768f.

– Arbuzov isomerization 31b-1985

– Arbuzov reaction 29-202, 288, 30-94f., 106, 669, 31b-1939, 1942, 1984–1986, 32-289, 442, 33-24, 75, 673

– Arbuzov reaction, modified 30-95

– Arbuzov rearrangement 31b-1985, 2041, 32-86

– Arbuzov-like intermediate 30-106

– Arbuzov-type reaction 30-672

– photo-Arbuzov reaction 31b-1942

Arduengo carbene

– Arduengo's carbene 31b-1708

B

Baeyer–Villiger oxidation

– Baeyer–Villiger oxidation 26-567, 29-675, 31a-292f., 410

– Baeyer–Villiger reaction 28-521

– Baeyer–Villiger-type reaction 26-108

Baldwin rule

– Baldwin rule 33-190

Balz–Schiemann reaction

– Baltz–Schiemann conditions 28-820

– Balz–Schiemann process 31a-61, 31b-1367

– Balz–Schiemann protocol 25-705

– Balz–Schiemann reaction 31a-56, 61

Bamberger rearrangement

– Bamberger rearrangement 31b-1644, 1654

– Bamberger-like reaction 31b-1571

Bamford–Stevens reaction

– Bamford–Stevens approach 28-822

– Bamford–Stevens reaction 27-872–883, 33-217

Barbier reaction

– Barbier conditions 26-260, 261

– Barbier cyclization 26-425

– Barbier reaction 29-124

– Barbier-type addition 32-150

– Barbier-type coupling 32-149

– Barbier-type procedure 26-260

– Barbier-type reaction 32-65

Barluenga's reagent

– Barluenga's reagent 31a-238, 243

Barton decarboxylation

– Barton decarboxylation 29-48, 808

Barton's reagent

– Barton's pyridylsulfanyl group 28-274

– Barton's reagent 28-332, 337

Barton–Pross–Sternhell procedure

– Barton–Pross–Sternhell procedure 29-105

Baylis–Hillman reaction

– aza-Baylis–Hillman reaction 33-508

– Baylis–Hillman adduct 26-1185, 1186, 31a-364

– Baylis–Hillman reaction 26-5, 404, 1094, 31a-364, 31b-1683, 33-41, 313

Béchamp reduction

– Béchamp reaction 31b-1621

– Béchamp reduction 31b-1621f.

Beckmann rearrangement

– Beckmann rearrangement 26-385, 27-631–634, 31a-767, 31b-1651f.

Bellus–Claisen rearrangement

– Bellus–Claisen rearrangement 29-80f.

benzidine rearrangement

– benzidine rearrangement 31b-1647, 1797, 1804

Birch reduction

– Birch reduction 31b-1627, 32-713, 33-221

– Birch reductive alkylation 31a-648

– retro-Birch reduction 31a-644

Birch–Wild–Nelson reduction

– Birch–Wild–Nelson reduction 26-216

Blaise reaction

– Blaise reaction 26-277, 1154

Bodroux–Chichibabin reaction

– Bodroux–Chichibabin reaction 29-554

Boeckman reaction

– Boeckman's conditions 29-665

Bohn–Schmidt oxidation

– Bohn–Schmidt oxidation 28-445

Bolm oxidation

– Bolm oxidation 31a-938

– Bolm system 31a-934

Borodin–Hunsdiecker reaction

– Borodin–Hunsdiecker reaction 29-132

Bredt's rule

– -Bredt nature 32-553

Brønstedt acid

– Brønstedt acid 25-4, 139, 151, 154–159, 164, 167–171, 184f., 187–190, 229, 408, 410f., 645, 717, 28-611, 29-151, 167, 171, 323, 356, 418, 427, 440–445, 451, 487, 540, 596, 681, 691, 817, 1064, 30-11, 38, 290, 297, 31a-262, 295, 297, 308, 322, 326, 609, 907, 31b-1209, 1464, 1466, 1827, 1839, 32-9, 540, 590, 33-347

– Brønstedt acidity 30-271

Brook rearrangement

– 1,3-Brook rearrangement 25-445

– Brook radical rearrangement 29-786

– Brook rearrangement 29-70, 820, 30-405

– Brook-type rearrangement 33-459

– retro-[1,4]-Brook rearrangement 29-843

Brown reaction

– Brown reaction 25-384, 386

Bucherer reaction

– Bucherer reaction 31b-1497, 1602, 1604f., 1812

– Bucherer-type reaction 31a-768

Buchwald method

– Buchwald method 31a-819

Buchwald–Hartwig reaction

– Buchwald–Hartwig amination 25-695, 698

– Buchwald–Hartwig aryl amination 33-415

– Buchwald–Hartwig reaction 31a-12f.

C

Cannizzaro reaction

– Cannizzaro reaction 25-355

– Cannizzaro-like hydride shift 25-424

Caro's acid

– Caro's acid 31b-1290, 1305, 1340f.

Carroll rearrangement

– Carroll rearrangement 26-1176

– Carroll rearrangement, asymmetric 33-522

Chapman rearrangement

– Chapman rearrangement 31b-1652

Chichibabin reaction

– Chichibabin reaction 31b-1565, 1572

Claisen condensation

– aza-Claisen condensation 33-572

– Claisen condensation 25-230, 28-417, 31a-364, 32-535, 579

– Claisen condensation, dual 28-417

– Claisen condensation, intramolecular 29-712

–...