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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
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
COC(=O)C1CC2C3CCC(=O)C3(C)CCC2C2(C)CCC(=O)CC12
Reaction #373697
DOI: 10.1039/C8SC04228D
CC(=O)OCC1CC2C3CCC(=O)C3(C)CCC2C2(C)CCC(=O)CC12
Reaction #1045649
DOI: 10.1039/C8SC04228D
COC[C@H]1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=NOCCN)CC12.Cl
Reaction #1999836
3-(2-Aminoethoxyimino)-6α-methoxymethylandrostan-17-one hydrochloride
Ausbeute 33.0%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
CC(=O)OC[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 #1999862
title compound
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
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 #1999867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC2C3CCC(=O)C3(C)CCC2C2(C)CCC(=NOCCN)CC12
Reaction #2408516
DOI: 10.1039/C8SC04228D