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402060

CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Reaction #1271
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)NCCCC[C@@H](C(=O)OC(C)(C)C)[NH+]([O-])C(=O)OCc1ccccc1
Reaction #1272
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CCN(C(=O)OCc2ccccc2)N1
Reaction #1426
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)OC(C)(C)C)cc2ccccc21
Reaction #41924
tert-butyl 2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)O)cc2ccccc21
Reaction #41925
2-(1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetic acid
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)C(C)C)ccc2n1CC(=O)OC(C)(C)C
Reaction #43858
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)C(C)C)ccc2n1CC(=O)O
Reaction #43859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)C3CCCCC3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43864
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)C3CCCCC3)ccc2n1CC(=O)O
Reaction #43865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(=O)n(C(=O)NCC2CCN(C3(C(=O)O)CCCCC3)CC2)c2ccccc21.Cl
Reaction #44884
1-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]cyclohexanecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC[C@H](NC(=O)c1cc(F)c(F)c(F)c1F)C(=O)OC(C)(C)C
Reaction #51888
di-tert-butyl (2,3,4,5-tetrafluorobenzoyl)-L-glutamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CCN2C(=O)CC[C@@H]2C(=O)OC(C)(C)C)cc1
Reaction #57045
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCC(=O)O)C(=O)CCC(Nc1ncnc2cc(C(=O)N3CCCC3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62441
6-chloro-4-[1-(5-chloro-1H-benzimidazol-2-yl)-3-(N-hydroxycarbonylethyl-N-methyl-amino-carbonyl)-propyl-amino]-7-(pyrrolidin-1-yl-carbonyl)-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)OCc2ccccc2)c(=O)n1CC(=O)OC(C)(C)C
Reaction #77151
title compound
Ausbeute 56.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NS(=O)(=O)Cc2ccccc2)c(=O)n1CC(=O)OC(C)(C)C
Reaction #77152
title compound
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77153
solid
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Cn1cccc(NS(=O)(=O)Cc2ccccc2)c1=O
Reaction #77160
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77161
solid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)OCc2ccccc2)c(=O)n1CC(=O)O
Reaction #77166
white solid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H]1CCCN1C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(N)=O)NC(=O)c1ccc2ccccc2c1
Reaction #82336
N-[2(R)-hydroxy-3(S)-[[N-(2-naphthoyl)-L-asparaginyl]amino]-4-phenylbutyl]-L-proline tert.butyl ester
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
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