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CC(=O)OC1CCC2(C)C(CCC3C4CCC(C#N)C4(C)CC(O)C32)C1
Reaction #262920
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C#N)CC[C@@H]12
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17β-Cyano-3α-hydroxy- 5α-androstane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C=C[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C#N)CC[C@@H]12
Reaction #354809
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC3C(CCC4CC(O)CCC43C)C1CCC2C#N
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DOI: 10.1039/C8SC04228D
CC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@H](O)C[C@]12C
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title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCC2C3CCC4CC(O)CCC4(C)C3C(O)CC12C
Reaction #2243148
DOI: 10.1039/C8SC04228D
C[C@]12C[C@H]3CC[C@@H]4C[C@@H](O)CC[C@@]4(C)[C@@H]3C[C@@H]1CC[C@@H]2C#N
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compound 28
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12C=CC(O)CC1CCC1C2CCC2(C)C(C#N)CCC12
Reaction #2401914
DOI: 10.1039/C8SC04228D