Teilstruktursuche

360781

C=C(C)C(=O)OCCO
Reaction #5381
2-hydroxyethyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 60.2%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
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)C(=O)[C@H]5C[C@H]5[C@H]4[C@@H]3[C@H](Cl)[C@H]3O[C@]32C1
Reaction #93692
3β-(tert.-butyldimethylsilyloxy)-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H]([C@@H](O)[C@H]4O[C@]45C[C@@H](O[Si](Cc4ccccc4)(Cc4ccccc4)Cc4ccccc4)CC[C@]35C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93695
3β-tribenzylsilyloxy-5,6β-epoxy-7β-hydroxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H]([C@H](Cl)[C@H]4O[C@]45C[C@@H](O[Si](Cc4ccccc4)(Cc4ccccc4)Cc4ccccc4)CC[C@]35C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93696
3β-tribenzylsilyloxy-7α-chloro-5,6β-epoxy-15β,16β-methylene-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C=CC(=O)C=C1[C@@H](F)C[C@H]1[C@@H]3C[C@@H](O)[C@](O)(C(=O)CO)[C@@]3(C)C[C@H](O)[C@@]12F
Reaction #155408
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC12CC(O)C3(F)C(CCC4=CC(=O)C=CC43C)C1CCC2S
Reaction #196202
DOI: 10.1039/C8SC04228D
C=C(COC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CCl)c1ccccc1
Reaction #199533
DOI: 10.1039/C8SC04228D
C=C(COC1CC2C3CCC4=CC(=O)CCC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO)c1ccccc1
Reaction #200009
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
CC(=O)OC1CC2(C)C(=O)CCC2C2CCC3=CC(=O)C=CC3(C)C12F
Reaction #212457
DOI: 10.1039/C8SC04228D
CCCOC(=O)C(=O)[C@@]1(O)[C@H](O)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #215039
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter