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CCCC1CCC(C2CCCCC2)CC1

CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49204
amide
Rendimiento 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49207
amide
Rendimiento 172.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCC(=O)[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](OC3CCCCO3)CC[C@@H]12
Reaction #55611
17β-tetrahydropyranyloxy-5α-androstan-4-one
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
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C(N)=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70368
title compound
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
Rendimiento 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
Rendimiento 46.0%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
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1C[C@@H](C(=O)O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70401
7α-carboxyandrostane-3,17-dione
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12
Reaction #70402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](N=[N+]=[N-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92529
3α-azidocholest-5-ene
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](N)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92530
3α-Aminocholest-5-ene
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCC(=O)C1CCC2C3CCC4CC(O)CCC4(C)C3C(=O)CC12C
Reaction #173818
DOI: 10.1039/C8SC04228D
CCC(C)(OC=CCC(C)(C)O[Si](CC)(CC)CC)C1=CCC2C3=CC=C4CC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C4(C)C3CCC12C
Reaction #190292
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2(C)C(=CC(=O)C3C4CCC(=O)C4(C)CCC32)C1
Reaction #198415
DOI: 10.1039/C8SC04228D
O=P(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #234925
DOI: 10.1039/C8SC04228D
CC(CCCO)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C
Reaction #235279
DOI: 10.1039/C8SC04228D
CC12CC(=O)C3C(CCC4CC(O)CCC43C)C1CCC2C(=O)CCCl
Reaction #238814
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2C3CCC4CC(N5CC(OS(C)(=O)=O)C5)CCC4(C)C3CCC12C
Reaction #253617
DOI: 10.1039/C8SC04228D
CC(=O)C1CCC2C3CCC4CC(O)(C#CCl)CCC4(C)C3CCC12C
Reaction #253835
DOI: 10.1039/C8SC04228D
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