L-tert-leucine

CC(C)(C)[C@H](N)C(N)=O
Reaction #6425
tertiary leucine amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #81111
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CC[C@@H]1C[C@H]1OC(=O)N[C@H](C(=O)O)C(C)(C)C.C[C@H](N)c1ccccc1
Reaction #88820
VII
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)[C@@H](N)C(=O)O
Reaction #164024
D-tert-leucine
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #322691
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #353025
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #443952
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC(C)(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #463636
CBZ-L-tert-leucine
المردود 200.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COC(=O)N[C@H](C(=O)O)C(C)(C)C
Reaction #467377
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
C=CCCCOC(=O)N[C@H](C(=O)O)C(C)(C)C
Reaction #475402
compound
المردود 147.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(S(=O)(=O)N[C@H](C(=O)O)C(C)(C)C)cc1
Reaction #498451
N-(Toluene-4-sulfonyl)-L-tert-butylglycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
Cc1ccccc1C(=O)NC(C(=O)O)C(C)(C)C
Reaction #566659
desired product
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC(C)(C)C(NC(=O)c1ccc(Cl)cc1)C(=O)O
Reaction #566661
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC(C)(C)C(NC(=O)c1ccccc1)C(=O)O
Reaction #566662
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC(C)(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O
Reaction #567389
CBZ-L-tert-leucine
المردود 200.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
C=CCC[C@@H]1CCC[C@H]1OC(=O)N[C@H](C(=O)O)C(C)(C)C
Reaction #609541
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CN1CCCn2c(Br)nc(C(=O)N[C@H](C(=O)N(C)C)C(C)(C)C)c2C1
Reaction #623151
(S)-3-bromo-N-(1-(dimethylamino)-3,3-dimethyl-1-oxobutan-2-yl)-8-methyl-6,7,8,9-tetrahydro-5H-imidazo[1,5-a][1,4]diazepine-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COC(=O)N[C@H](C(=O)O)C(C)(C)C
Reaction #730238
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(C)(C)[C@H](NC=O)C(=O)O
Reaction #742383
(S)-2-Formylamino-3,3-dimethyl-butyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #830101
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
الصفحة 1التالي