Drayton / Backes / Bellus Index Volume Category 5

1. Auflage 2013
ISBN: 978-3-13-178571-8
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 1000 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 2009.

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 5 Cumulative Index – Compounds with One Saturated Carbon–Heteroatom Bond;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;42
1.7.1;Compounds with One C–X Bond: Monocyclic Compounds;42
1.7.2;Compounds with One C–X Bond: Bicyclic Compounds;82
1.7.3;Compounds with One C–X Bond: Tricyclic Compounds;116
1.7.4;Compounds with One C–X Bond: Tetracyclic Compounds;137
1.7.5;Compounds with One C–X Bond: Pentacyclic Compounds;149
1.7.6;Compounds with One C–X Bond: Hexacyclic Compounds;156
1.7.7;Compounds with One C–X Bond: Octacyclic Compounds;159
1.7.8;Compounds with One C–X Bond: Undecacyclic Compounds;160
1.7.9;Compounds with One C–X Bond: Polycyclic Compounds;161
1.8;Name Reaction Index;162
1.8.1;A;162
1.8.2;B;162
1.8.3;C;163
1.8.4;D;164
1.8.5;E;165
1.8.6;F;165
1.8.7;G;166
1.8.8;H;166
1.8.9;I;167
1.8.10;J;167
1.8.11;K;167
1.8.12;L;168
1.8.13;M;168
1.8.14;N;170
1.8.15;O;171
1.8.16;P;171
1.8.17;R;172
1.8.18;S;172
1.8.19;T;174
1.8.20;U;174
1.8.21;V;174
1.8.22;W;174
1.8.23;Y;175
1.8.24;Z;175
1.9;Keyword Index;176
1.9.1;A;176
1.9.2;B;300
1.9.3;C;322
1.9.4;D;346
1.9.5;E;370
1.9.6;F;402
1.9.7;G;407
1.9.8;H;414
1.9.9;I;438
1.9.10;J;448
1.9.11;K;448
1.9.12;L;458
1.9.13;M;460
1.9.14;N;468
1.9.15;O;477
1.9.16;P;494
1.9.17;Q;556
1.9.18;R;556
1.9.19;S;558
1.9.20;T;588
1.9.21;U;610
1.9.22;V;611
1.9.23;W;611
1.9.24;X;612
1.9.25;Y;612
1.9.26;Z;613
1.10;Author Index;614
1.10.1;A;614
1.10.2;B;630
1.10.3;C;663
1.10.4;D;688
1.10.5;E;706
1.10.6;F;713
1.10.7;G;727
1.10.8;H;748
1.10.9;I;774
1.10.10;J;781
1.10.11;K;790
1.10.12;L;823
1.10.13;M;843
1.10.14;N;879
1.10.15;O;893
1.10.16;P;902
1.10.17;Q;923
1.10.18;R;924
1.10.19;S;942
1.10.20;T;987
1.10.21;U;1006
1.10.22;V;1009
1.10.23;W;1018
1.10.24;X;1036
1.10.25;Y;1037
1.10.26;Z;1045
1.11;Abbreviations;1054
1.12;List of All Volumes;1060

Leseproben

Name Reaction Index

A

Abushanab modification

– Abushanab modification 37-415f.

Adams' catalyst

– Adams' catalyst 41-492

Aggarwal's asymmetric annulation

– Aggarwal's asymmetric annulation 37-354

Aidhen's synthesis

– Aidhen's synthesis 37-709

Alder-ene reaction

– Alder-ene reaction 37-602f.

Aldol reaction

– Aldol acceptor 36-767

– Aldol addition 36-448, 546, 847–858, 861f., 869–879, 885, 887, 891, 898–900, 902–905, 907–925, 927f., 928–943, 947–950

– Aldol adduct 36-847, 852, 857, 866, 868–871, 876, 897, 898, 930–934, 37-381

– Aldol condensation 36-497, 920

– Aldol donor 36-767

– Aldol method 36-847, 848

– Aldol product 36-847

– Aldol reaction 36-102, 498, 546, 765, 849, 860, 872, 876, 903, 907–913, 920–922, 927f., 931– 933, 936, 37-155, 385, 719, 40a-841

– Aldol reaction, asymmetric 42-939

– Aldol reaction, diastereoselective, direct 36-766

– Aldol reaction, enantioselective, direct 36-766

– Aldol reaction, intramolecular 36-876

– Aldol–reduction sequence 36-780f.

– Aldol–ring-closing metathesis 37-550f.

– Aldol-type condensation 36-271

– Aldol-type reaction 36-889

– anti-Aldol reaction 36-860

– Aza-aldol reaction 40a-689

– Cross-aldol addition 36-869, 923

– Cross-aldol reaction 36-938–940, 42-939, 940

– Direct aldol reaction 36-766, 767

– exo-Aldol cyclization 36-919

– Nitro-aldol reaction 36-498

– Self-aldolization 36-856

– syn-Aldol reaction 36-860

– syn-Aldol, Evans 36-875

– syn-Aldol, non-Evans 36-875

– Tandem Michael addition–aldol reaction 36-498

Alpine-Borane

– Alpine-Borane (Midland's reagent) 36-540

Appel's reagent

– Appel's reagent 42-969

Arbuzov reaction

– Arbuzov reaction 41-226, 42-227, 229, 607, 645, 746

– Arbuzov rearrangement 42-253

– Arbuzov-type reaction 42-642, 645, 662, 663

– Arbuzov-type rearrangement 42-260, 609

– Thia-Arbuzov reaction 39-220

Atherton–Todd reaction

– Atherton–Todd conditions 42-916

– Atherton–Todd reaction 42-715

B

Baeyer–Villiger oxidation

– Baeyer–Villiger oxidation 37-284, 310, 38-35, 453, 40a-483, 489

– Baeyer–Villiger product 39-689

– Baeyer–Villiger reaction 38-449

Baker–Venkataraman rearrangement

– Baker–Venkataraman rearrangement 37-761

Baldwin's rules

– Baldwin's rules 37-444

Bamberger rearrangement

– Bamberger rearrangement 40a-391, 392

Barbier reaction

– Barbier conditions 36-277, 307, 1147

– Barbier coupling 37-788f.

– Barbier reaction 37-785, 788f.

– Barbier-type addition 36-327

– Barbier-type conditions 37-375

– Barbier-type reaction 36-278, 37-40, 40a-325

– Barbier-type reaction, intramolecular 36-506

Barbier–Grignard reaction

– Barbier–Grignard reaction 36-278

Barbier–Reformatsky reaction

– Barbier–Reformatsky conditions 36-497

– Barbier–Reformatsky-type reaction 36-496

Barton reaction

– Barton alkenation 39-683

– Barton ester method 35-565

– Barton esters 35-569, 41-544

– Barton reaction 41-281

Barton-type cyclization

– Barton-type cyclization 38-243

Barton–McCombie reaction

– Barton–McCombie reaction 34-6

Baylis–Hillman reaction

– Aza-Baylis–Hillman reaction 40a-597–600, 42-381

– Baylis–Hillman acetate 40b-973, 41-552–554

– Baylis–Hillman adduct 35-712

– Baylis–Hillman reaction 36-498, 41-238, 42-352, 935

Beaucage's reagent

– Beaucage's reagent 42-876, 877, 880–882, 899

Beckmann rearrangement

– Beckmann procedure 40a-394

– Beckmann rearrangement 40a-393

Beller catalyst

– Beller catalytic system 37-228, 267f.

Bellus–Claisen rearrangement

– Aza-Bellus–Claisen rearrangement 40a-759

Bennek's procedure

– Bennek's procedure 37-667

Birch reduction

– Birch reduction 36-39, 75, 38-373, 39-1100

– Birch-type conditions 36-602

– Birch-type reaction 36-128

Blank reaction

– Blank reaction 35-159

Bouveault reduction

– Bouveault reduction 36-146

Bouveault–Blanc reduction

– Bouveault–Blanc reduction 36-75, 128

Boyer reaction

– Boyer reaction 41-598, 599

– Tandem Diels–Alder/Boyer reaction 41-598

Brassard's diene

– Brassard's diene 40a-354

Braun reaction

– Braun's methodology 36-856

Bredt rule

– Anti-Bredt bridgehead 40a-140

– Bredt's rule 40b-845

Brigl's anhydride

– Brigl's anhydride 37-771

Brønsted acid

– Brønsted acid 35-251, 36-58, 94, 95, 107, 112, 122, 504, 972, 976, 1031, 37-19, 20, 23, 26, 47, 72, 74, 158, 260, 382, 396, 436, 441, 461, 492, 594, 599, 38-44, 51–53, 73, 130, 453, 39-515f., 519, 522, 529, 872, 1089, 40a-72, 107, 319, 324, 343, 351, 438, 452, 462, 602, 666, 724, 730, 732, 733, 41-598, 634, 42-381, 469, 477, 513, 941

– Brønsted acid, chiral 37-594, 40a-107, 438, 452

– Brønsted acid–base conditions 36-217

– Brønsted acidic ionic liquid 40a-73

– Brønsted acidity 38-166

– Brønsted relationship 39-885

Brønsted base

– Brønsted base 36-399, 430, 37-381

Brook reaction

– Brook reaction 36-1150

– Retro-Brook reaction 36-1150

Brook rearrangement

– Brook rearrangement 36-474

– 1,2-Brook rearrangement 36-1150

– Retro-Brook rearrangement 36-1130

Buchanan reaction

– Buchanan's method 37-715

– Buchanan's synthesis 37-712f.

Buchwald reaction

– Buchwald cross coupling 42-406

– Buchwald ligand 42-425

– Buchwald-type ligand 42-380

Buchwald–Hartwig reaction

– Buchwald–Hartwig aryl amination 42-381

– Buchwald–Hartwig methodology 42-358

Bunte salts

– Bunte salts 39-30, 393, 394, 581, 897

Burgess epoxidation

– Burgess epoxidation 37-251

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