Поиск подструктуры

535014

NCCN
Reaction #2024
ethylenediamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](O)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40591
8a
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40592
10
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40593
13
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OS(C)(=O)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40594
white solid
Выход 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](O[Si](C)(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40595
16
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=N)C(Cl)(Cl)Cl)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40596
21
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)Nc2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40597
22
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40598
34
Выход 81.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40599
35
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](Br)C(=O)[C@@H]2[C@@]3(C)C[C@@H](c4ccoc4)OC(=O)[C@H]3CC[C@]21C
Reaction #40600
36
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H](C(=O)N(C)C)CC1
Reaction #44989
methyl trans-4-[(dimethylamino)carbonyl]-cyclohexanecarboxylate
Выход 87.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@H](C(=O)O)CC1
Reaction #44990
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC12CCC(C(=O)OC)(CC1)CC2
Reaction #51107
methyl 4-pentylbicyclo[2.2.2]octane-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC12CCC(C(=O)Cl)(CC1)CC2
Reaction #51112
4-pentylbicyclo[2.2.2]octane-1-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC12CCC(C(=O)NC)(CC1)CC2
Reaction #51113
N-methyl-4-pentylbicyclo[2.2.2]octane-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1-c1cc(C(=O)NC2(C(=O)O)C3CC4CC(C3)CC2C4)nn1-c1cccc2ccccc12
Reaction #65479
2-{[1-(1-Naphthyl)-5-(2,6-dimethoxyphenyl)-3-pyrazolyl]-carbonylamino}-2-adamantanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C(=O)O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70367
6α-carboxyandrostane-3,17-dione
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C(N)=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70369
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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