Substructure Search

16349

COc1ccc([C@@H](NC(=O)OC(C)(C)C)C(=O)O)cc1C
Reaction #61111
(R)-tert-butoxycarbonylamino-(4-methoxy-3-methyl-phenyl)-acetic acid
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cn(CC(Cl)(C(=O)c2ccc(Cl)cc2Cl)c2ccccc2)cn1)C(=O)O
Reaction #62768
1-[2-chloro-3-(2,4-dichlorophenyl)-3-oxo-2-phenylpropyl]-N-[ (1,1-dimethylethoxy)carbonyl]-L-histidine
Yield 48.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)[C@H](Cc1cn(CC(Cl)(C(=O)c2ccc(Cl)cc2Cl)c2ccccc2)cn1)NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #62769
N-[1-[2-chloro-3-(2,4-dichlorophenyl)-3-oxo-2-phenylpropyl]-N-[(1,1-dimethylethoxy)carbonyl]-L-histidyl]-L-alanine 1,1-dimethylethyl ester
Yield 89.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CCCN)C(=O)O
Reaction #80673
Boc-Orn-OH
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(NC(=O)OC(C)(C)C)(C(=O)OCC)C(=O)OCC
Reaction #86024
title compound
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C[C@@](NC(=O)OC(C)(C)C)(C(=O)O)C(=O)OCC
Reaction #86025
title compound
Yield 108.4%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
Yield 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
COc1ccc([C@@H](O)[C@H](NC(=O)OC(C)(C)C)C(=O)O)cc1
Reaction #87143
(2S,3R)-2-(tert-butoxycarbonylamino)-3-hydroxy-3-(4-methoxyphenyl)propanoic acid
Yield 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #87144
(2S,3R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-hydroxy-3-(4-methoxyphenyl)propanoate
Yield 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(N)C(=O)c1ccc(OC)cc1
Reaction #87147
methyl 2-amino-3-(4-methoxyphenyl)-3-oxopropanoate
Yield 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CCN(Cc2ccccc2)CC1
Reaction #92582
crude product
Yield 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(NN)CCN(Cc2ccccc2)CC1.Cl
Reaction #92583
crude product
Yield 88.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Oc1ccc(CC(N)C(=O)OC(C)COC(=O)c2ccccc2)cc1OC(=O)OCC
Reaction #188833
DOI: 10.1039/C8SC04228D
NC(CC(=O)N1CCOCC1)C(=O)OCc1ccccc1
Reaction #192866
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(CNc1ccccc1N)C(=O)O
Reaction #200521
DOI: 10.1039/C8SC04228D
C=CCOc1ccc(CC(NC(=O)OC(C)(C)C)C(=O)O)cc1F
Reaction #206236
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(OCc2ccccc2)cc1CO)NC(=O)OC(C)(C)C
Reaction #219349
3-(4-benzyloxy-2-hydroxymethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2cc(OCc3ccccc3)ccc2CC(NC(=O)OC(C)(C)C)C1=O
Reaction #219350
(8-benzyloxy-2-methyl-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-4-yl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(OCc2ccccc2)cc1CO)NC(=O)OC(C)(C)C
Reaction #219483
3-(4-benzyloxy-2-hydroxymethyl-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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