Recherche de Sous-structure

516987

C=CCOC[C@H](C(=O)OC(C)(C)C)[C@H](O)COC(C)=O
Reaction #48321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@@H](COC(C)=O)O[Si](C)(C)C(C)(C)C
Reaction #48322
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](N(C)C)[C@H]2O)[C@](C)(O)C[C@@H](C)CN(C)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #52549
Azithromycin monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64079
t-butyl (3S)-2-methyl-3-hydroxybutanoate
Rendement 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)[C@H](C)[C@@H](C)O
Reaction #64081
isopropyl (2R, 3R)-2-methyl-3-hydroxybutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)[C@H](C)[C@H](C)O
Reaction #64084
isopropyl (2R, 3S)-2-methyl-3-hydroxybutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C(=O)OC(C)(C)C)[C@H](C)O
Reaction #64085
t-butyl (3S )-2-ethyl-3-hydroxybutanoate
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65120
N-demethylerythromycin A
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #65121
N-demethylerythromycin A
Rendement 40.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C(Cc1ccc(Cl)c(Cl)c1)C(=O)OC(C)(C)C
Reaction #81137
tert-butyl (2RS, 3RS)-2-(3,4-dichlorobenzyl)-3-hydroxybutanoate
Rendement 35.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C(CO)Cc1ccc(Cl)c(Cl)c1
Reaction #81138
(2RS, 3RS)-2-(3,4-dichlorobenzyl)-1,3-butanediol
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O[Si](C)(C)C(C)(C)C)C(CO)Cc1ccc(Cl)c(Cl)c1
Reaction #81145
(2RS, 3RS)-2-(3,4-dichlorobenzyl)-3-(tert-butyldimethylsilyloxy)butanol
Rendement 76.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C[C@H](C(=O)OC(C)C)[C@@H](O)C(=O)OC(C)C)nc(-n2c(C)ccc2C)c1
Reaction #160664
4b
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H](C(=O)OC(C)C)[C@H](Cc1cc(C)cc(-n2c(C)ccc2C)n1)C(=O)OC(C)C
Reaction #160665
10
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H](CO)[C@@H](CO)Cc1cc(C)cc(-n2c(C)ccc2C)n1
Reaction #160666
11
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H](C=O)[C@H](Cc1cc(C)cc(-n2c(C)ccc2C)n1)C(=O)OC(C)C
Reaction #160667
16
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H](CNCc1ccccc1)[C@H](Cc1cc(C)cc(-n2c(C)ccc2C)n1)C(=O)OC(C)C
Reaction #160668
19
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO[C@@H](CNCc1ccccc1)[C@@H](CO)Cc1cc(C)cc(-n2c(C)ccc2C)n1
Reaction #160669
20
Rendement 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@H](NC)[C@H]2O)[C@](C)(O)C[C@@H](C)CN(C)[C@H](C)[C@@H](O)[C@]1(C)O
Reaction #164457
amine
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(CC1OC(=O)C1CCCCCC)OC1CCCCO1
Reaction #176364
DOI: 10.1039/C8SC04228D
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