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1260555

CCOC(=O)C1C2CCC(=O)C21
Reaction #1861
title compound
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2CCC(=O)C21
Reaction #1862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2CCC(=O)C21
Reaction #173318
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=CC[C@@H]2[C@H]1[C@@]2(F)C(=O)OCC
Reaction #217679
(1R,5R,6R)-6-fluoro-bicyclo[3.1.0]hex-2-ene-2,6-dicarboxylic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(C(=O)OCc2ccccc2F)CC(O)C2C(C(=O)OCc3ccccc3F)C21
Reaction #248247
DOI: 10.1039/C8SC04228D
C=C1CC(NC(=O)OCc2ccccc2)(C(=O)OCC)C2C1C2C(=O)OCC
Reaction #275239
DOI: 10.1039/C8SC04228D
COC(=O)C1(F)C2C(=O)CC(O[Si](C)(C)C(C)(C)C)C21
Reaction #288050
DOI: 10.1039/C8SC04228D
O=C(O)C1C2CCC(=O)C21
Reaction #373692
DOI: 10.1039/C8SC04228D
COC(=O)C1(F)C2C(=O)CC(O)C21
Reaction #385292
DOI: 10.1039/C8SC04228D
O=C(O)C1C2CCC(=O)C21
Reaction #389513
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C2(N1)C1CC3C2C3(C(=O)O)C1
Reaction #440556
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(F)[C@@H]2[C@@H](OC(C)=O)CC(=O)[C@@H]21
Reaction #490108
Methyl (1S,2S,5R,6R)-2-(acetyloxy)-6-fluoro-4-oxobicyclo [3.1.0] hexane-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557089
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557090
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(C(=O)OC(C)(C)C)[C@@H]2[C@@H](C(=O)OC(C)(C)C)[C@@H]2C(=O)[C@H]1CSc1ccc(F)c(F)c1
Reaction #557091
di-tert-butyl (1S,2R,3S,5R,6R)-2-[(tert-butoxycarbonyl)amino]-3-{[(3,4-difluorophenyl)sulfanyl]methyl}-4-oxobicyclo[3.1.0]hexane-2,6-dicarboxylate
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(C(=O)OC(C)(C)C)[C@@H]2[C@@H](C(=O)OC(C)(C)C)[C@@H]2[C@H](O)[C@H]1CSc1ccc(F)c(F)c1
Reaction #557092
title compound
Ausbeute 60.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SC[C@@H]2[C@H](O)[C@H]3[C@H](C(=O)OC(C)(C)C)[C@H]3[C@]2(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)ccc1F
Reaction #557093
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557101
title compound
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(=O)[C@H]2[C@H](C(=O)OC(C)(C)C)[C@H]2[C@]1(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #557102
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@]1(C(=O)OC(C)(C)C)[C@@H]2[C@@H](C(=O)OC(C)(C)C)[C@@H]2C(=O)[C@H]1CSc1ccc(F)c(F)c1
Reaction #557103
title compound
Ausbeute 141.0%DOI: 10.6084/m9.figshare.5104873.v1
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