Substructure Search

$CO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12$

Reaction #70378

17,17-Bis(ethylendioxy)-5α-hydroxy-6-(E)-hydroxyimino-androstane

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CCCC[C@]34C)[C@@H]1CC13OCCOC12OCCO3$

Reaction #70382

Yield 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

$CO/N=C1\C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O$

Reaction #70384

C[C@H](N)CON=C1CC[C@@]2(C)C(CC[C@H]3[C@@H]4CCC[C@@]4(C)CC[C@@H]32)C1.C[C@]12CCCCC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.Cl

Reaction #1999840

Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #1999841

Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #1999868

$CO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12$

Reaction #1999869

$CCO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12$

Reaction #1999871

Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1

$C=CCO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12$

Reaction #1999872

17,17-Bis(ethylendioxy)-5α-hydroxy-6-(E)-hydroxyiminoandrostane

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CCCC[C@]34C)[C@@H]1CC13OCCOC12OCCO3$

Reaction #1999884

Yield 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 #1999885

$CO/N=C1\C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O$

Reaction #1999886