Teilstruktursuche

CCCCCCCCC(=O)CCCCCCCC

C[C@]12CC[C@H]3[C@@H](CC[C@@H]4CC(O)CC[C@@H]43)[C@@H]1CCC21OCCO1
Reaction #7508
title compound
Ausbeute 94.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)[C@@H](N5CCCCC5)C[C@@H]34)[C@@]2(C)C[C@@H]1N1CCCCC1
Reaction #65119
(2β,3α,5α,16β)-3-acetyloxy-2,16-di-(1-piperidinyl)androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](SC3CCNC3)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.O=C(O)/C=C/C(=O)O
Reaction #70354
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45C[C@@H](O)CC[C@]35C)[C@@H]1CCC2=O
Reaction #70359
3β-hydroxy-5α,6α-epoxyandrostane-17-one
Ausbeute 47115.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC[C@@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2O
Reaction #70360
androstane-3β,5α,17β-triol
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45CCCC[C@]35C)[C@@H]1CCC2=O
Reaction #70379
5α,6α-epoxyandrostan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC(=O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70380
5α-hydroxyandrostane-3,6,17-trione
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70386
3β-hydroxyandrostane-7,17-dione
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93689
7α-chloro-5,6β-epoxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3C=C[C@]2(O)C1
Reaction #93690
5-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androst-6-en-17-one
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93692
3β-(tert.-butyldimethylsilyloxy)-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(C)C
Reaction #93693
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H]([C@@H](O)[C@H]4O[C@]45C[C@@H](O[Si](Cc4ccccc4)(Cc4ccccc4)Cc4ccccc4)CC[C@]35C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93695
3β-tribenzylsilyloxy-5,6β-epoxy-7β-hydroxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H]([C@H](Cl)[C@H]4O[C@]45C[C@@H](O[Si](Cc4ccccc4)(Cc4ccccc4)Cc4ccccc4)CC[C@]35C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93696
3β-tribenzylsilyloxy-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(C)C
Reaction #93697
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(CC[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)OCC)OC(C)(C)C
Reaction #95267
desired product
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CC[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)OCC
Reaction #95268
15-hydroxy-9-oxoprostanoic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4CC(=O)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95330
17β-acetoxy-1α-methyl-17α-n-propyl-5α-androstan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95331
17β-acetoxy-1α-methyl-17α-n-propyl-5α-androstan-3β-ol
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter