Ähnlichkeitssuche

686356

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
CCOC(=O)C(CC(=O)OC(C)C)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #86021
title compound
Ausbeute 102.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OC(C)(C)C)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #86022
title compound
Ausbeute 100.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OCc1ccccc1)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #86023
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OC(C)(C)C)(C(N)=O)C(=O)OCC
Reaction #86026
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86027
title compound
Ausbeute 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(=O)OCC
Reaction #86029
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@](CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(=O)O
Reaction #86030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@](CC(=O)OCc1ccccc1)(NC(=O)OC(C)(C)C)C(N)=O
Reaction #86031
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@]1(NC(=O)OC(C)(C)C)CC(=O)NC1=O
Reaction #86032
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)CNC(=O)OCc1ccccc1
Reaction #298486
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(C#N)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #343781
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NC(=O)OCc2ccccc2)CC(=O)NC1=O
Reaction #343782
title compound
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(C)(C)CNC(=O)OCc1ccccc1
Reaction #352133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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