Recherche de Sous-structure

12866

CC(=O)OCC(=O)[C@@]1(O[Si](C)(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42650
title compound
Rendement 103.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42651
title compound
Rendement 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)O[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42652
title compound
Rendement 62.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42653
(11β,16β)-9-fluoro-11,21-dihydroxy-16-methyl-3,20-dioxopregna-1,4-dien-17-yl ethylcarbamate
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)O[C@]1(C(=O)COC(C)=O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42654
(11β,16β)-21-(acetyloxy)-9-fluoro-11-hydroxy-16-methyl-3,20-dioxopregna-1,4-dien-17-yl ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C)c1ccccc1
Reaction #42655
(11β,16β)-9-fluoro-11,21-dihydroxy-16-methyl-3,20-dioxopregna-1,4-dien-17-yl (1R)-1-phenylethylcarbamate
Rendement 57.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42656
title compound
Rendement 60.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)CC2=C(C1)C(=O)C=CC2=O
Reaction #64368
title compound
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #70500
solid
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C(Cc2ccc(CCCC(=O)N3CCOCC3)cc2)=C(C)C1=O
Reaction #76671
title compound
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81347
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-3,20-dioxo-9-fluoro-16β-methyl-17-valeroyloxy-pregna -1,4-dien-21-yl] ester
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1=C(CC[C@](C)(O)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=O)C(C)=C(C)C1=O
Reaction #92090
(R,R,R)-2-allyl-3-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5,6-dimethyl-[1,4]benzoquinone
Rendement 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1=C(CC[C@](C)(O)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C(=O)C(C)=C(C)C1=O
Reaction #92091
(R,R,R)-2-(3-hydroxy-3,7,11,15-tetramethyl-hexadecyl)-5,6-dimethyl-3-propyl-[1,4]benzoquinone
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(OC)C(=O)C2=C(CCC(CCOc3ccc(C)cc3)CC2)C1=O
Reaction #180070
DOI: 10.1039/C8SC04228D
COC(=O)C1(OC(=O)c2ccc(O)o2)C(C)CC2C3CC(F)C4=CC(=O)C=CC4(C)C34OC4CC21C
Reaction #185648
DOI: 10.1039/C8SC04228D
CCCNC(=O)OC1(C(=O)CO)C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC21C
Reaction #203830
DOI: 10.1039/C8SC04228D
CC12C=CC(=O)C=C1C(F)CC1C3CC4CN(Cc5ccccc5)CC4(C(=O)SC4CCOC4=O)C3(C)CC(O)C12F
Reaction #207496
DOI: 10.1039/C8SC04228D
C=C1C=C(OCC)C(=O)C(OCC)=C1
Reaction #211587
DOI: 10.1039/C8SC04228D
CC(C)(C)C1=CC(=Nc2cnccn2)C=C(C(C)(C)C)C1=O
Reaction #211855
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(C(=O)OC)CC(C)=C(C)C1
Reaction #215948
title compound
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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