tyrosine methyl ester

CC(C)C[NH2+][C@H](CCl)Cc1ccc(O)cc1.[Cl-]
Reaction #363679
N-((1S)-1-(4-hydroxyphenylmethyl)-2-chloroethyl)-N-isobutylammonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
COC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](C)NC(=O)Cc1cc(F)cc(F)c1
Reaction #409890
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COC(=O)C(Cc1ccc(O)cc1)NC(=O)N(CCCl)CCCl
Reaction #438317
30
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCOP(=O)(CCCCc1ccccc1)CC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)OC
Reaction #521591
N-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-tyrosine, methyl ester
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
O=C(CCCNC(=O)NC1CCCCC1)NC(Cc1ccc(O)cc1)C(=O)O
Reaction #531855
target product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](C)NC(=O)Cc1cc(F)cc(F)c1
Reaction #723341
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
COC(=O)[C@@H](N)Cc1ccc(O[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)cc1
Reaction #937324
O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester
Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_01
COC(=O)C(Cc1ccc(O)cc1)NC(C)=CC(=O)c1ccccc1
Reaction #1003319
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)NC(C)=CC(=O)c1ccc(F)cc1
Reaction #1003322
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)NC(C)=CC(=O)c1cccnc1
Reaction #1003325
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1ccccc1
Reaction #1003328
title compound
Ausbeute 40.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1ccc(F)cc1
Reaction #1003331
title compound
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1cccnc1
Reaction #1003334
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1ccc(C(C)(C)C)cc1
Reaction #1003341
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1ccc(C)cc1
Reaction #1003344
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)C(Cc1ccc(O)cc1)Nc1ccccc1C(=O)c1ccccc1C
Reaction #1003347
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_09
COC(=O)[C@H](Cc1ccc(O)cc1)Nc1nc(-c2ccccc2)cs1
Reaction #1057266
methyl(2S)-3-(4-hydroxyphenyl)-2-[(4-phenyl-1,3-thiazol-2-yl)amino]propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
COC(=O)[C@H](Cc1ccc(O)cc1)Nc1nc(-c2ccc(C#N)cc2)cs1
Reaction #1057270
Methyl (2S)-2-{[4-(4-cyanophenyl)-1,3-thiazol-2-yl]amino}-3-(4-hydroxyphenyl)propionate
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
COC(=O)[C@H](Cc1ccc(O)cc1)Nc1nc(-c2ccc(C)cc2)cs1
Reaction #1057271
Methyl (2S)-2-{[4-(4-methylphenyl)-1,3-thiazol-2-yl]amino}-3-(4-hydroxyphenyl)propionate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_12
COC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](C)NC(=O)Cc1cc(F)cc(F)c1
Reaction #1070441
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_03
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