Index Volume Category 5 (eBook)
Thieme (Verlag)
978-3-13-178571-8 (ISBN)
Science of Synthesis: Category 5 Cumulative Index – Compounds with One Saturated Carbon–Heteroatom Bond 1
Imprint 5
Title page 6
List of All Volumes 7
Preface 12
Table of Contents 14
Product Class Overview 16
Structure Index 42
Compounds with One C–X Bond: Monocyclic Compounds 42
Compounds with One C–X Bond: Bicyclic Compounds 82
Compounds with One C–X Bond: Tricyclic Compounds 116
Compounds with One C–X Bond: Tetracyclic Compounds 137
Compounds with One C–X Bond: Pentacyclic Compounds 149
Compounds with One C–X Bond: Hexacyclic Compounds 156
Compounds with One C–X Bond: Octacyclic Compounds 159
Compounds with One C–X Bond: Undecacyclic Compounds 160
Compounds with One C–X Bond: Polycyclic Compounds 161
Name Reaction Index 162
A 162
B 162
C 163
D 164
E 165
F 165
G 166
H 166
I 167
J 167
K 167
L 168
M 168
N 170
O 171
P 171
R 172
S 172
T 174
U 174
V 174
W 174
Y 175
Z 175
Keyword Index 176
A 176
B 300
C 322
D 346
E 370
F 402
G 407
H 414
I 438
J 448
K 448
L 458
M 460
N 468
O 477
P 494
Q 556
R 556
S 558
T 588
U 610
V 611
W 611
X 612
Y 612
Z 613
Author Index 614
A 614
B 630
C 663
D 688
E 706
F 713
G 727
H 748
I 774
J 781
K 790
L 823
M 843
N 879
O 893
P 902
Q 923
R 924
S 942
T 987
U 1006
V 1009
W 1018
X 1036
Y 1037
Z 1045
Abbreviations 1054
List of All Volumes 1060
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
–...
| 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 • synthetic transformations |
| ISBN-10 | 3-13-178571-3 / 3131785713 |
| ISBN-13 | 978-3-13-178571-8 / 9783131785718 |
| Haben Sie eine Frage zum Produkt? |
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