Nε -Carbobenzyloxy-L-lysine

Cc1ccc(S(=O)(=O)NC(CCCCNC(=O)OCc2ccccc2)C(=O)O)cc1
Reaction #6465
title compound
Ausbeute 81024.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N[C@@H](CC(Cc1ccccc1)C(=O)O)C(=O)O.N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #92811
γ-benzyl-L-glutamic acid Nε-benzyloxycarbonyl-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCCCCCCCCCCC(=O)OC(CCCCCCCCCCCCCCC)CC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #323687
Nα -(3-hexadecanoyloxyoctadecanoyl)-Nε -benzyloxycarbonyl-L-lysine
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCCCCCCCCCCCCCCC(=O)OC(CCCCCCCCCCCCCCC)CC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #323688
Nα -[Nα -(3-hexadecanoyloxyoctadecanoyl)-Nε -benzyloxycarbonyl-L-lysyl]-Nε -benzyloxycarbonyl-L-lysine
Ausbeute 67.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #417236
BOC-Leu-Lys(Z)
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
N[C@@H](CC(=O)O)C(=O)O
Reaction #546248
Asp
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
O=C(NCCCC[C@H](NC(=O)C(F)(F)F)C(=O)O)OCc1ccccc1
Reaction #565300
2-N-Trifluoroacetyl-6-N-benzyloxycarbonyl-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CS(=O)(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #655127
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
O=C(NCCCCC1NC(=O)OC1=O)OCc1ccccc1
Reaction #682713
Lys-NCA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOC(=O)[C@@H](N)CCCCNC(=O)OCc1ccccc1
Reaction #724468
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_12
CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)O
Reaction #1060567
BOC-Leu-Lys(Z)
Ausbeute 72.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
CC(C)(C)OC(=O)[C@@H](N)CCCCNC(=O)OCc1ccccc1
Reaction #1066359
t-butyl Nε-benzyloxycarbonyl-L-lysinate
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
N[C@@H](CC(=O)O)C(=O)O
Reaction #1153559
Asp
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
C1CCC(NC2CCCCC2)CC1.O=C(NCCCC[C@H](NS(=O)(=O)c1ccccc1)C(=O)O)OCc1ccccc1
Reaction #1161197
Nα -benzenesulfonyl-Nε -benzyloxycarbonyl-L-lysine dicyclohexylamine salt
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
C1CCC(NC2CCCCC2)CC1.O=C(NCCCC[C@H](NS(=O)(=O)c1ccccc1[N+](=O)[O-])C(=O)O)OCc1ccccc1
Reaction #1161199
Nα -o-nitrobenzenesulfonyl-Nε -benzyloxycarbonyl-L-lysine dicyclohexylamine salt
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
Cc1ccc(S(=O)(=O)NC(CCCCNC(=O)OCc2ccccc2)C(=O)O)cc1
Reaction #1815959
title compound
Ausbeute 81024.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_07
O=C(NCCCC[C@H](NC(=O)C(F)(F)F)C(=O)O)OCc1ccccc1
Reaction #1925970
2-N-trifluoroacetyl-6-N-benzyloxycarbonyl-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_01
CC(C)(C)OC(=O)[C@@H](N)CCCCNC(=O)OCc1ccccc1
Reaction #2069549
t-butyl Nε-benzyloxycarbonyl-L-lysinate
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_06
O=C(NCCCC[C@H](Nc1nc2ccc(Cl)cc2cc1C(=O)O)C(=O)O)OCc1ccccc1
Reaction #2152786
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
NCCCC[C@@H](C(=O)O)N(CC(=O)O)CC(=O)O
Reaction #2375302
Nα,Nα -bis (carboxymethyl)-L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_07
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