Boc-Leu-H

C=CC(O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #4352
desired product
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
C=CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #4355
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)CC(CNC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #366062
(1-{[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethylamino]-methyl}-3-methyl-butyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)CC(CNC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #366074
oil
المردود 12.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)CC(CNC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #366076
oil
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #433084
desired product
المردود 38.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
CC(C)CC(CNC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #516309
(1-{[2-(4-benzyloxy-phenyl)-1-tert-butylcarbamoyl-ethylamino]-methyl}-3-methyl-butyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)CC(CNC(Cc1ccc(OCc2ccccc2)cc1)C(=O)NC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #516315
oil
المردود 12.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)C[C@@H](CO)NC(=O)OC(C)(C)C
Reaction #521664
BOC-leucinol
المردود 76.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(O)c1nccs1
Reaction #563981
(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-methyl-1-(2-thiazolyl)-1-pentanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
CCOC(=O)C(F)(F)[C@H](O)[C@H](CC(C)C)NC(=O)OC(C)(C)C
Reaction #1061106
N--BOC--(4S,3R)-2,2-difluorostatine ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
CC(C)C[C@@H](CN1CCN(C(c2ccc(F)cc2)c2ccc(F)cc2)CC1)NC(=O)OC(C)(C)C
Reaction #1077545
pure titled compound
المردود 41.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_10
CC(C)C[C@H](NC(=O)OC(C)(C)C)[C@H](O)c1nccs1
Reaction #1117704
(S)2-(t-butoxycarbonyl)amino-4-methyl-(S)1-(2-thiazolyl)pentan-1-ol
المردود 4.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
CC(C)C[C@H](NC(=O)OC(C)(C)C)[C@@H](O)c1ncnn1C
Reaction #1117706
(S)2-(tert-butoxycarbonyl)amino-4-methyl-(R)1-(1-methyl-1H-1,2,4-triazol-5 -yl)pentan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
CC(C)CC(NC(=O)OC(C)(C)C)[C@@H](O)c1ccccn1
Reaction #1117707
( S )
المردود 21.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
CC(C)=CCN(c1ccc(OCc2ccccc2)cc1)C1CCN(C[C@@H](N)CC(C)C)CC1
Reaction #1156639
desired product
المردود 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
CCOC(=O)CC(O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #1174777
desired product
المردود 38.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_07
C=CC(CC(C)C)NC(=O)OC(C)(C)C
Reaction #1174785
3-t-butyloxycarbonylamino-5-methylhex-1-ene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_07
CC(C)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NN=[N+]=[N-])C(=O)NN
Reaction #1340591
Compound 38
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(C)O
Reaction #1485564
tert-butyl ((3S)-2-hydroxy-5-methylhexan-3-yl)carbamate
المردود 71.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
الصفحة 1التالي