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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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 85.0%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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O
Reaction #70381
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70383
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CO/N=C1\C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O
Reaction #70384
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C/C(=N\O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70390
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CO/N=C1\CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70391
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCO/N=C1\CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70392
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70394
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](CO)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70396
7α-Hydroxymethylandrostane-3,17-dione
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@H](CO)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70397
7β-Hydroxymethylandrostane-3,17-dione
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
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