(S)-α-ethylbenzylamine

CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](NC(=O)OCc1ccccc1)C(Cc1ccccc1)C(=O)O)[C@H](C)CC)c1ccccc1
Reaction #865
N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
収率 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50343
secondary amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC[C@H](NC(=O)c1c(O)c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #364143
title compound
収率 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)C1(C(C#N)N[C@@H](CC)c2ccccc2)CC1
Reaction #429229
diastereomer mixture
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC[C@H](NC(=O)c1c(C)c(-c2ccccc2)nc2cc(OC)ccc12)c1ccccc1
Reaction #438909
(S)-N-(α-Ethylbenzyl)-3-methyl-7-methoxy-2-phenylquinoline-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
CC[C@H](NC(=O)c1c(C)c(-c2ccccc2)nc2cc(OC)ccc12)c1ccccc1
Reaction #483530
(S)-N-(α-Ethylbenzyl)-3-methyl-7-methoxy-2-phenylquinoline-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CC[C@H](N=C=O)c1ccccc1
Reaction #538151
(S)-(1-isocyanatopropyl)benzene
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCC[C@H](NC(=O)OC(C)(C)C)[C@H](O)C(=O)N[C@@H](CC)c1ccccc1
Reaction #722820
3(S)-(tert-butoxyformamido)-2(S)-hydroxy-N-(1(S)-phenylpropyl)heptanamide
収率 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
CC[C@H](NC(=O)c1c(O)c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #738236
title compound
収率 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CC[C@H](NC(=O)c1c(N)c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #738237
title compound
収率 78.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CC[C@H](NC(=O)c1c(NS(C)(=O)=O)c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #743087
title compound
収率 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC[C@H](NC(=O)c1c(CN=[N+]=[N-])c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #743093
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC[C@H](NC(=O)Cc1ccccc1C(=O)O)c1ccccc1
Reaction #971921
title compound
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC[C@H](NC(=O)c1cc(C(=O)N[C@@H](CC)c2ccccc2)n2c1OCCC2)c1ccccc1
Reaction #1013588
3,4-dihydro-2H-pyrrolo[2,1-b][1,3]oxazine-6,8-dicarboxylic acid bis-[((S)-1-phenyl-propyl)-amide]
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CC[C@H](NC(=O)c1c(O)c(-c2ccccc2)nc2ccccc12)c1ccccc1.Cl
Reaction #1337226
light beige product
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_01
C[C@H](NCc1ccccc1)c1ccccc1
Reaction #1539052
N-benzyl-(S)-α-methylbenzylamine
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_02
CC[C@H](NCCC1(O)CCC2(CC1)OCC(C)(C)CO2)c1ccccc1
Reaction #1702337
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CC[C@H](NC(=O)Nc1ccc(Oc2ccnc3cc(OC)c(OC)cc23)cc1)c1ccccc1
Reaction #1904601
title compound
収率 121.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
CC[C@H](NC(=O)c1c(NS(C)(=O)=O)c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #1909242
title compound
収率 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
CC[C@H](NC(=O)c1c(CN=[N+]=[N-])c(-c2ccccc2)nc2ccccc12)c1ccccc1
Reaction #1909248
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
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