(S)—N-(tert-butoxycarbonyl)-tert-leucine

CCOC(=O)[C@H](C)NC[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #72423
desired compound
수율 43.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(=O)O
Reaction #72424
desired compound ( 20 )
수율 191.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N[C@](Cc1ccccc1)(C(=O)O)C(C)(C)C
Reaction #162888
title compound
수율 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc2c(c1)CN(C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)[C@H](C(=O)N[C@@H]1CCCc3ccccc31)C2
Reaction #426414
title compound
수율 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)N[C@H](C(=O)N1Cc2cc([N+](=O)[O-])ccc2C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21)C(C)(C)C
Reaction #426435
title compound
수율 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)N[C@H](C(=O)N[C@@H](CC1CCCC1)C(=O)OCc1ccccc1)C(C)(C)C
Reaction #449328
N-[N-(tert-butoxycarbonyl)-3-methyl-L-valyl]-3-cyclopentyl-L-alanine benzyl ester
수율 61.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CC(C)(C)OC(=O)NC(C(=O)N1CCC2C1C(C(=O)Nc1cccc3ccccc13)CN2C(=O)CNC(=O)OCc1ccccc1)C(C)(C)C
Reaction #534172
57
수율 109.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #560732
desired compound
수율 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
C[C@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(=O)O
Reaction #560733
desired compound ( 20 )
수율 191.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)OC(=O)N[C@H](C(=O)Nc1cc(I)ccc1N)C(C)(C)C
Reaction #607545
(S)-tert-butyl (1-((2-amino-5-iodophenyl)amino)-3,3-dimethyl-1-oxobutan-2-yl)carbamate
수율 104.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CN(C)C(=O)[C@@H](NCc1cccc(C(C)(C)C)c1O)C(C)(C)C
Reaction #607953
2h
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC(C)(C)OC(=O)N[C@@H](C(=O)OCc1ccccc1)C(C)(C)C
Reaction #624560
(R)-benzyl 2-(tert-butoxycarbonylamino)-3,3-dimethylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CNC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #652417
(2S)-2-tert-butoxycarbonylamino-3,3-dimethylbutanoic acid methylamide
수율 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC(C)(C)OC(=O)N[C@H](C(=O)NCc1ccccn1)C(C)(C)C
Reaction #652431
(2S)-2-tert-butoxycarbonylamino-3,3-dimethylbutanoic acid 2-pyridylmethylamide
수율 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
—
Reaction #710534
solid
수율 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)OC(=O)N[C@H](C(=O)N[C@@H](CC1CCCC1)C(=O)OCc1ccccc1)C(C)(C)C
Reaction #938072
N-[N-(tert-butoxycarbonyl)-3-methyl-L-valyl]-3-cyclopentyl-L-alanine benzyl ester
수율 61.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
CNC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C
Reaction #975127
(2S)-2-tert-butoxycarbonylamino-3,3-dimethylbutanoic acid methylamide
수율 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC(C)(C)OC(=O)NC(C(=O)N1CCCC1C(=O)OCc1ccccc1)C(C)(C)C
Reaction #987753
title compound
수율 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
CO[C@H]([C@@H](C)C(=O)N[C@H](C(=O)N1CCCCO1)C(C)(C)C)[C@@H]1CCCN1C(=O)OC(C)(C)C
Reaction #1109702
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccc(-c2ccccn2)cc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)C(C)(C)C
Reaction #1261397
title compound
수율 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
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