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9487

CC[C@H](NC(=O)C(CC)(CC)NC(=O)[C@@H](N)CC(=O)O)c1ccccc1
Reaction #867
α-L-aspartyl-α,α-diethylglycine (S)-α-ethylbenzylamide
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](NC(=O)[C@@H](C)NC(=O)[C@@H](N)CC(=O)O)c1ccccc1
Reaction #874
α-L-aspartyl-D-alanine-(R)-α-methoxymethylbenzylamide
Ausbeute 57.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)OCc1ccccc1)C(=O)Nn1cccc1
Reaction #50655
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)OCc1ccccc1)C(=O)Nn1cccc1
Reaction #50658
product
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](N)C(=O)Nn1cccc1
Reaction #50659
desired product
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)OCc1ccccc1)C(=O)Nn1cccc1
Reaction #50664
desired product
Ausbeute 90.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N)C(=O)Nn1cccc1
Reaction #50665
product
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](O)[C@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #53965
(2S,3S)-2-{[(benzyloxy)carbonyl]amino}-3-hydroxy-4-methylpentanoic acid
Ausbeute 109.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(CCNC(=O)C(NC(=O)OCc1ccccc1)C(O)C(C)C)OCC
Reaction #53966
[1-(3,3-diethoxy-propylcarbamoyl)-2-hydroxy-3-methyl-butyl]-carbamic acid benzyl ester
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OCc1ccccc1)P(O)O
Reaction #54264
1-carbobenzyloxyamino-2-methylpropanephosphonous acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCNC(=O)OC(C)(C)C)OP(=O)(OC)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #58021
2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)O
Reaction #75317
N-benzyloxycarbonyl-L-alanyl-L-alanine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)NCc1ccccc1)C(C)C
Reaction #82441
desired product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccc([N+](=O)[O-])cc1)C(=O)O
Reaction #83094
desired product
Ausbeute 35.7%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(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
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