Substructure Search

303232

CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C
Reaction #928
17β-Acetoxy-2,3-dihydroxyimino-5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC[C@@H]4CC(=O)CC[C@@H]43)[C@@H]1CC[C@@H]2O
Reaction #7507
title compound
Yield 107.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CCC45OC4C(=O)CC[C@H]35)[C@@H]1CC/C2=C\Cl
Reaction #52574
E-17-Chloromethylene-4ξ,5ξ-epoxy-estran-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C
Reaction #55323
cholesta-1,4-dien-3-one
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #70362
solid
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70363
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](CO)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70364
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[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 #70365
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70366
6α-Formylandrostane-3,17-dione
Yield 85.0%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
Yield 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
C[C@]12CCC(=O)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70370
title compound
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[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 #70371
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](NC=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70372
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C(=C(F)F)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70373
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C#C[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 #70374
title compound
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](CCO)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70377
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12
Reaction #70378
title compound
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
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