Recherche de Sous-structure

CCCCCCCCCCCCCCCCCC(C)=O

O=C(NC1CCCCC1)NC1CCCCC1
Reaction #55696
dicyclohexylurea
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #55697
dicyclohexylurea
Rendement 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #55698
dicyclohexylurea
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #55699
dicyclohexylurea
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)OC(O)C(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81343
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methylbutyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester
Rendement 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](N)C(=O)OC(O)C(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C.O=C(O)C(F)(F)F
Reaction #81344
(2S)-2-amino-3-methyl-butyric acid [11β,17,21-trihydroxy-3,20-dioxo-pregn-4-en-21-yl] ester trifluoroacetate
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)CCC2C3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@@]21C
Reaction #86293
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC(=C)[C@@]3(O)C(C)=O)[C@@]2(C)CCC(=O)C=C12
Reaction #93684
17α-Acetyl-17β-hydroxy-6,16-dimethyleneandrosta-4-en-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H]2[C@H](CC[C@]3(C)C(C(C)=O)=C(CS(=O)c4ccccc4)C[C@@H]23)[C@@]2(C)CCC(=O)C=C12
Reaction #93685
6-Methylene-16-(phenylsulfinylmethyl)pregna-4,16-diene-3,20-dione
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC(=C)[C@]3(O)C(C)=O)[C@@]2(C)CCC(=O)C=C12
Reaction #93686
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4CC(=O)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95330
17β-acetoxy-1α-methyl-17α-n-propyl-5α-androstan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@]1(OC(C)=O)CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)C[C@H](C)[C@]4(C)[C@H]3CC[C@@]21C
Reaction #95331
17β-acetoxy-1α-methyl-17α-n-propyl-5α-androstan-3β-ol
Rendement 64.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(C)C(=O)CC[C@@H]12
Reaction #167597
11β-Hydroxy-4-androstene-3,17-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1CCC2C3CCC4CC(O)CCC4(C)C34OC4CC12C
Reaction #174125
DOI: 10.1039/C8SC04228D
CC(=O)C1CCC2C3CCC4CC(O)C(C)CC4(C)C3C(=O)CC12C
Reaction #174790
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2(C)C(CCC3C4CCC(C(C)=O)C4(C)CC(OC(=O)CCl)C32)CC1O
Reaction #203174
DOI: 10.1039/C8SC04228D
CC12CCC(=O)C=C1CCC1C2CCC2(C)C1CCC2(O)C(=O)CCl
Reaction #209314
DOI: 10.1039/C8SC04228D
CC(=O)C1CCC2C3CCC4CC(O)C(O[N+](=O)[O-])CC4(C)C3C(=O)CC12C
Reaction #212020
DOI: 10.1039/C8SC04228D
CC(=O)C1CCC2C3CCC4CC(OC(=O)c5cccnc5)CCC4(C)C3CCC12C
Reaction #233306
DOI: 10.1039/C8SC04228D
CCCCC1CC(=O)C2(C)CCC3=C4CCC(=O)C=C4CCC3C12
Reaction #233992
DOI: 10.1039/C8SC04228D
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