N-methoxycarbonyl-L-Valine

COC(=O)N[C@H](C(=O)O)C1CC1
Reaction #84036
(S)-2-cyclopropyl-2-(methoxycarbonylamino)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC[C@H](C)[C@H](NC(=O)OC)C(=O)O
Reaction #84037
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)NC(C(=O)O)C1CCOCC1
Reaction #84038
2-(methoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)N[C@H](C(=O)O)[C@@H](C)OC
Reaction #84039
(2S,3R)-3-methoxy-2-(methoxycarbonylamino)butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)N[C@H](C(=O)O)C1CCCC1
Reaction #84042
(S)-2-cyclopentyl-2-(methoxycarbonylamino)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC[C@@H](C)[C@H](NC(=O)OC)C(=O)O
Reaction #84043
(2S,3R)-2-(methoxycarbonylamino)-3-methylpentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)N[C@H](C(=O)N1CCC[C@H]1c1ncc(-c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)[nH]1)C(C)C
Reaction #158855
(S,S)-[2-methyl-1-(2-{5-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-propyl]-carbamic acid methyl ester
Выход 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc3c(c2)CN(C)Cc2cc(-c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)ccc2-3)[nH]1)C(C)C
Reaction #166834
(1-{2-[5-(9-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-6-methyl-6,7-dihydro-5H-dibenzo[c,e]azepin-3-yl)-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl]-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC[C@H](C)[C@H](NC(=O)OC)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2cncs2)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #467383
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC[C@H](C)[C@H](NC(=O)OC)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2nccs2)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #467393
1-[4-(Thiazol-2-yl)-phenyl]-4(S)-hydroxy-2-N-(N-methoxycarbonyl-(L)-valyl)amino-5(S)-N-(N-methoxycarbonyl-(L)-iso-leucyl)amino-6-phenyl-2-azahexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2nnn(C(C)(C)C)n2)cc1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C(C)C
Reaction #467405
1-[4-(2-tert-Butyl-2H-tetrazol-5-yl)-phenyl]-4(S)-hydroxy-2-N-(N-methoxycarbonyl-(L)-tert-leucyl)amino-5(S)-N-(N-methoxycarbonyl-(L)-valyl)amino-6-phenyl-2-azahexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CON[C@H](C(=O)NN(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=O
Reaction #467416
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC[C@H](C)[C@H](NC(=O)OC)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)[C@@H](NOC)C(C)C=C=O
Reaction #467419
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc3c(c2)CN(C)Cc2cc(-c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)ccc2-3)[nH]1)C(C)C
Reaction #504588
(1-{2-[5-(9-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-6-methyl-6,7-dihydro-5H-dibenzo[c,e]azepin-3-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)N[C@H](C(=O)N1CCC[C@H]1c1nc(-c2ccc(-c3ccc(-c4c[nH]c([C@@H]5CC6(CN5C(=O)[C@@H](NC(=O)OC)C(C)C)OCCCO6)n4)cc3)cc2)c[nH]1)C(C)C
Reaction #541602
Methyl [(1S)-2-methyl-1-({(2S)-2-[4-(4′-{2-[(3S)-2-((2S)-3-methyl-2-{[(methyloxy)carbonyl]amino}butanoyl)-6,10-dioxa-2-azaspiro[4.5]dec-3-yl]-1H-imidazol-4-yl}-4-biphenylyl)-1H-imidazol-2-yl]-1-pyrrolidinyl}carbonyl)propyl]carbamate
Выход 55.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)C1CC2(CCOCC2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #541604
product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COC(=O)N[C@H](C(=O)N1CC2(CCC(F)(F)CC2)C[C@H]1C(=O)O)C(C)C
Reaction #541611
title compound
Выход 93.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)C1CC2(CCN(C(=O)OC(C)(C)C)CC2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #541614
title compound
Выход 55.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)C1CC2(CN(C(=O)OC(C)(C)C)C2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #541620
title compound
Выход 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCOC(=O)C1CC2(CCOCC2)CN1C(=O)[C@@H](NC(=O)OC)C(C)C
Reaction #622304
product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
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