Index Volume Category 4 (eBook)
Thieme (Verlag)
978-3-13-178551-0 (ISBN)
Science of Synthesis: Category 4 Cumulative Index – Compounds with Two Carbon–Heteroatom Bonds 1
Imprint 5
Title page 6
List of All Volumes 7
Preface 12
Table of Contents 14
Product Class Overview 16
Structure Index 40
Aldehydes, Ketones, and Derivatives: Monocyclic Compounds 40
Aldehydes, Ketones, and Derivatives: Bicyclic Compounds 83
Aldehydes, Ketones, and Derivatives: Tricyclic Compounds 123
Aldehydes, Ketones, and Derivatives: Tetracyclic Compounds 160
Aldehydes, Ketones, and Derivatives: Pentacyclic Compounds 180
Aldehydes, Ketones, and Derivatives: Hexacyclic Compounds 191
Aldehydes, Ketones, and Derivatives: Heptacyclic Compounds 194
Aldehydes, Ketones, and Derivatives: Octacyclic Compounds 198
Aldehydes, Ketones, and Derivatives: Nonacyclic and Higher Compounds 199
Name Reaction Index 202
A 202
B 202
C 203
D 204
E 205
F 205
G 206
H 207
I 208
J 208
K 208
L 209
M 209
N 211
O 211
P 211
R 212
S 213
T 214
U 214
V 215
W 215
Y 216
Z 216
Keyword Index 218
A 218
B 345
C 396
D 422
E 467
F 497
G 502
H 511
I 525
J 537
K 537
L 562
M 564
N 573
O 590
P 601
Q 667
R 670
S 671
T 709
U 731
V 732
W 734
X 735
Y 735
Z 736
Author Index 738
A 738
B 756
C 797
D 828
E 851
F 859
G 878
H 902
I 935
J 944
K 953
L 993
M 1019
N 1065
O 1081
P 1094
Q 1119
R 1120
S 1144
T 1202
U 1228
V 1231
W 1243
X 1264
Y 1265
Z 1276
Abbreviations 1286
List of All Volumes 1292
Name Reaction Index
A
Achmatowicz reaction
– Achmatowicz reaction 29-372
– Achmatowicz ring expansion 29-457
Adams reaction
– Adams modification 31a-441
Alder cis-principle
– Alder cis-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
– anti-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
–...
| Erscheint lt. Verlag | 11.12.2013 |
|---|---|
| Reihe/Serie | Science of Synthesis | Science of Synthesis |
| Verlagsort | Stuttgart |
| Sprache | englisch |
| Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
| Technik | |
| Schlagworte | chemistry of organic compound • chemistry organic reaction • CHEMISTRY ORGAN IC REACTION • chemistry reference work • chemistry synthetic methods • Compound • compound functional group • compound organic synthesis • Functional Group • Mechanism • Method • methods in organic synthesis • METHODS IN O RGANIC SYNTHESIS • methods peptide synthesis • Organic Chemistry • organic chemistry functional groups • ORGANIC CHEMIST RY FUNCTIONAL GROUPS • organic chemistry reactions • organic chemistry review • organic chemistry synthesis • organic method • organic reaction • organic reaction mechanism • Organic Syntheses • organic synthesis • organic synthesis reference work • ORGANIC SYNTHESIS REFERENCE WO RK • Peptide synthesis • Practical • practical organic chemistry • Reaction • reference work • Review • review organic synthesis • review synthetic methods • Synthetic Methods • Synthetic Organic Chemistry • synthetic transformation • SYNTHETIC TRA NSFORMATION |
| ISBN-10 | 3-13-178551-9 / 3131785519 |
| ISBN-13 | 978-3-13-178551-0 / 9783131785510 |
| Haben Sie eine Frage zum Produkt? |
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