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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@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[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[C@H]1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC24OCCOC23OCCO4)[C@@]2(C)CCCCC12
Reaction #70375
17,17-Bis(ethylendioxy)-6α-vinylandrostane
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1[C@@H](CCO)C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70376
17,17-Bis(ethylendioxy)-6α-(2-hydroxyethyl)androstane
Ausbeute 96.0%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
C[C@]12CCCCC1C[C@H](CO)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70395
17,17-bis(ethylendioxy)-7β-hydroxymethylandrostane
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1C[C@@H](NC=O)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #70399
17,17-Bis(ethylendioxy)-7α-formamidoandrostane
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1[C@H](O[N+](=O)[O-])C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #1999843
17,17-Bis(ethylendioxy)androstane-6β-yl nitrate
Ausbeute 50.0%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 #1999855
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 #1999856
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C[C@H]1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC24OCCOC23OCCO4)[C@@]2(C)CCCCC12
Reaction #1999857
17,17-Bis(ethylendioxy)-6α-vinylandrostane
Ausbeute 70.0%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 #1999858
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1[C@@H](CCO)C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3
Reaction #1999859
17,17-Bis(ethylendioxy)-6α-(2-hydroxyethyl)androstane
Ausbeute 96.0%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 #1999860
title compound
Ausbeute 100.0%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 #1999861
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 #1999863
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
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