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258312

CCCC1CCC(C(C(=O)OCC)C(=O)OCC)CC1=O
Reaction #42599
2-(3-oxo-4-propylcyclohexyl)-malonic acid diethyl ester
Rendimiento 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C1CCCC(=O)C1
Reaction #42600
(3-Oxo-cyclohexyl)-malonic acid diethyl ester
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1CCCC(=O)C1
Reaction #42601
(3-Oxo-cyclohexyl)-acetic acid
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCC2C3CCC4CC(O)C(OC)CC4(C)C3C(=O)CC12C
Reaction #277910
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C(=O)OCC)C1CCCC(=O)C1
Reaction #299614
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@@H](O)C[C@@H]1CC[C@H]1[C@@H]3CC[C@H](C(=O)O)[C@@]3(C)CC(=NO)[C@@H]12
Reaction #310615
title compound
Rendimiento 63.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354792
17β-Ethoxycarbonyl-3α-hydroxy-5α-androstan-11-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354793
3α-Hydroxy-17β-isopropoxycarbonyl-5α-androstan-11-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)[C@@H](OC)C[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354795
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)[C@@H](Br)C[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=C[C@@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354797
3β-hydroxy-17β-methoxycarbonylandrost-4-en-11-one
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354798
title compound
Rendimiento 29.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354799
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCOC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354800
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354801
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](O)C[C@@H]1CC[C@H]1[C@@H]3CC[C@H](C(=O)OCC#N)[C@@]3(C)CC(=O)[C@@H]12
Reaction #354802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@](C)(O)CC[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354804
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)C=C[C@]4(C)[C@H]3C(=O)C[C@]12C
Reaction #354805
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](O)C[C@@H]1CC[C@H]1[C@@H]3CC[C@H](C(=O)OCCCN4CCOCC4)[C@@]3(C)CC(=O)[C@@H]12
Reaction #354806
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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