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CCCOCCCl

COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #1859
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOCCOc1ccc(C(=O)O)cc1
Reaction #11500
title compound
Ausbeute 105.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F
Reaction #64739
colorless liquid
DOI: 10.6084/m9.figshare.5104873.v1
O=CC(F)(OC(F)(F)C(F)(F)C(F)(F)F)C(F)(F)F
Reaction #64743
liquid
Ausbeute 53.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(OC(=O)CCl)C(C)n1ncn(-c2ccc(N3CCN(c4ccc(OCC5COC(Cn6cncn6)(c6ccc(F)cc6F)O5)cc4)CC3)cc2)c1=O
Reaction #76756
2-[4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-4,5-dihydro-5-oxo-1H-1,2,4-triazol-1-yl]-1-methylpropyl chloroacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCC2(CC1)OCC(CN1C(=O)c3ccccc3C1=O)O2
Reaction #80677
title compound
Ausbeute 101.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1OC(C(Cl)(Cl)Cl)N[C@H]1c1ccccc1
Reaction #82192
(4S,5R)-5-methoxycarbonyl-4-phenyl-2-trichloromethyl-1,3-oxazolidine
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87478
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cc2cc([C@]34OC[C@](CCl)(O3)[C@@H](O)[C@H](O)[C@H]4O)ccc2Cl)cc1
Reaction #87498
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)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 #93689
7α-chloro-5,6β-epoxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)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]3C=C[C@]2(O)C1
Reaction #93690
5-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androst-6-en-17-one
Ausbeute 74.6%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
CC(C)OC(C)C
Reaction #93693
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C=C[C@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1[C@@H]1C[C@@H]1C2=O
Reaction #93694
3β,5-dihydroxy-15β,16β-methylene-5β-androst-6-en-17-one
Ausbeute 94.4%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
CC(C)OC(C)C
Reaction #93697
diisopropyl ether
DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1O[C@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)C(Cl)(Cl)Cl
Reaction #162017
trichloroacetimidate
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(OC1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H](O[C@H]2O[C@H](COC(=O)c3ccccc3)[C@@H](OC(=O)c3ccccc3)[C@H](O[C@H]3O[C@H](COC(=O)c4ccccc4)[C@@H](OC(=O)c4ccccc4)[C@H](OC(=O)c4ccccc4)[C@@H]3OC(=O)c3ccccc3)[C@@H]2OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)C(Cl)(Cl)Cl
Reaction #162023
trichloroacetimidate
Ausbeute 72.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #162026
foam
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
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