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1081471

CCOC(=O)C(=O)C(Cc1cc(OC)ccc1Br)C(=O)OCC
Reaction #5440
desired product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Sc2ccccc2)C1C(=O)OC
Reaction #6068
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(S(=O)(=O)c2ccccc2)C1C(=O)OC
Reaction #6069
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H]1C[C@H]1C(=O)O
Reaction #48728
desired compound
Ausbeute 88.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CCc1ccccc1)C(C(=O)OCC)C(=O)OCC
Reaction #58047
2-ethoxycarbonyl-3-phenethyl-succinic acid diethyl ester
Ausbeute 52.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)C(Cc1ccc(NC(=O)OC(C)(C)C)nc1)(C(=O)OCC)C(=O)OCC
Reaction #58048
2-(6-tert-butoxycarbonylamino-pyridin-3-ylmethyl)-3-butyl-2-ethoxycarbonyl-succinic acid diethyl ester
Ausbeute 78.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(S(=O)(=O)O)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65789
title compound
Ausbeute 152.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NC(=O)OCc1ccccc1)(C(=O)OCC)C(=O)OCC
Reaction #86013
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NC(=O)OCc1ccccc1)(C(=O)OCC)C(=O)OCC
Reaction #86014
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OCc1ccccc1)(C(=O)O)C(=O)OCC
Reaction #86015
(R)-1-ethyl hydrogen 3-benzyloxycarbonylamino-3-ethoxycarbonylsuccinate
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OCc1ccccc1)(C(=O)O)C(=O)OCC
Reaction #86016
(R)-1-ethyl hydrogen 3-benzyloxycarbonylamino-3-ethoxycarbonylsuccinate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OCc1ccccc1)(C(N)=O)C(=O)OCC
Reaction #86017
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OCc2ccccc2)CC(=O)NC1=O
Reaction #86018
title compound
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OC)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #86020
title compound
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](CN(Cc1ccccc1)C(=O)OCc1ccccc1)[C@H](CC=O)C(=O)OC(C)(C)C
Reaction #89698
1-methyl 4-tert-butyl(2R,3S)-2-({benzyl[(benzyloxy)cabonyl]amino}methyl)-3-(2-oxoethyl)butanedioate
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@H]1CC(=O)CN(C(=O)OCc2ccccc2)[C@@H]1C(=O)OCc1ccccc1
Reaction #89704
ketone
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C1C[C@H](C(=O)OC(C)(C)C)[C@@H](C(=O)OCc2ccccc2)N(C(=O)OCc2ccccc2)C1
Reaction #89705
1,2-dibenzyl 3-tert-butyl(2S,3S)-5-(2-methoxy-2-oxoethylidene)piperidine-1,2,3-tricarboxylate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CN[C@H](C(=O)O)[C@@H](C(=O)OC(C)(C)C)C1
Reaction #89706
(2S,3S)-3-(tert-butoxycarbonyl)-5-(2-methoxy-2-oxoethyl)piperidine-2-carboxylic acid
Ausbeute 88.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@@H](O)CC[C@@H]1C(=O)OC(C)(C)C
Reaction #89772
desired product
Ausbeute 88.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CC(CNC2CC2)CC[C@@H]1C(=O)OC(C)(C)C
Reaction #89773
desired product
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1
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