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697862

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(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(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #244137
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(NC(=O)OCc1ccccc1)(C(=O)OCC)C(=O)OCC
Reaction #558519
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 #558520
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 #558521
(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 #558522
(R)-1-ethyl hydrogen 3-benzyloxycarbonylamino-3-ethoxycarbonylsuccinate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)OC)(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #558526
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 #558527
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 #558528
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 #558529
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)OCc1ccccc1)C(=O)OCC
Reaction #564390
diethyl 2-(N-benzyloxycarbonylamino)malonate
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCC(NC(=O)OCc1ccccc1)(C(=O)O)C(=O)OCC
Reaction #666684
2-(benzyloxycarbonylamino)-2-(ethoxycarbonyl)hex-5-enoic acid
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(CC)CC)(NC(=O)OCc1ccccc1)C(=O)O
Reaction #789835
DOI: 10.1039/C8SC04228D
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