Recherche de Sous-structure

391261

O=S1(=O)CCCc2ccc(CCCCOCCCCCCBr)cc21
Reaction #208453
DOI: 10.1039/C8SC04228D
C=CCCOCCCCCCBr
Reaction #398404
DOI: 10.1039/C8SC04228D
CC(=CCC(OC(=O)CC(O[Si](C)(C)C(C)(C)C)C(C)(C)C(=O)C(C)Br)C(C)=Cc1csc(C)n1)CCCC(C)C=O
Reaction #1037552
DOI: 10.1039/C8SC04228D
CC1=CCC(C(C)=Cc2csc(C)n2)OC(=O)CC(O[Si](C)(C)C(C)(C)C)C(C)(C)C(=O)C(C)C(O)C(C)CCC1
Reaction #1071715
4-(Tert-butyl-dimethyl-silanyloxy)-8-hydroxy-5,5,7,9,13-pentamethyl-16-[1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-oxacyclohexadec-13-ene-2,6-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=CCC(OC(=O)C[C@H](O[Si](C)(C)C(C)(C)C)C(C)(C)C(=O)C(C)Br)C(C)=Cc1csc(C)n1)CCCC(C)C=O
Reaction #1071718
(3S)-6-Bromo-3-(tert-butyl-dimethyl-silanyloxy)-4,4-dimethyl-5-oxo-heptanoic acid-4,8-dimethyl-1-[1-methyl-2-(2-methyl-thiazol-4-yl)-vinyl]-9-oxo-non-3-enyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC3C(CC4OC45CC=CCC35C)C1CC=C2Br
Reaction #1225349
DOI: 10.1039/C8SC04228D
O=S1(=O)CCCc2ccc(CCCCOCCCCCCBr)cc21
Reaction #1680216
title compound
Rendement 37.9%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccnc1CCCCOCCCCCCBr
Reaction #2195212
title compound
Rendement 99.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCOCCCCCCBr
Reaction #2205517
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45CC=CC[C@]35C)[C@@H]1CC=C2Br
Reaction #2507419
5α,6α-epoxy-17-bromo-androsta-2,16-diene
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1