Teilstruktursuche

1092214

COC(=O)C(Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1N
Reaction #283754
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1NCc1cccc2ccccc12
Reaction #399448
DOI: 10.1039/C8SC04228D
CCC(C)CNc1ccc(Cl)cc1C(=O)NC(Cc1ccc(Br)cc1)C(=O)OC
Reaction #761038
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1NCc1ccc2ccccc2c1
Reaction #776609
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(-c2ccc(C(F)(F)F)cc2)cc1)NC(=O)c1cc(Cl)ccc1N
Reaction #1038741
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1N
Reaction #1332285
2-(2-amino-5-chloro-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl ester
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(-c2ccc(C(F)(F)F)cc2)cc1)NC(=O)c1cc(Cl)ccc1N
Reaction #1332288
2-(2-amino-5-chloro-benzoylamino)-3-(4′-trifluoromethyl-biphenyl-4-yl)-propionic acid methyl ester
Ausbeute 122.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1332290
product
Ausbeute 93.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1NCc1ccc2ccccc2c1
Reaction #1332295
3-(4-Bromo-phenyl)-2-{5-chloro-2-[(naphthalen-2-ylmethyl)-amino]-benzoylamino}-propionic acid methyl ester
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)CNc1ccc(Cl)cc1C(=O)NC(Cc1ccc(-c2ccccc2OCc2ccccc2)cc1)C(=O)O
Reaction #1641859
DOI: 10.1039/C8SC04228D
COC(=O)[C@H](Cc1ccc(Br)cc1)NC(=O)c1cc(Cl)ccc1NCc1cccc2ccccc12
Reaction #1871420
(S)-3-(4-Bromo-phenyl)-2-{5-chloro-2-[(naphthalen-1-ylmethyl)-amino]-benzoylamino}-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccc(-c2ccc(Oc3ccccc3)cc2)cc1)C(=O)O)c1cc(Cl)ccc1NCc1cccc2ccccc12
Reaction #1871421
title compound
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)CNc1ccc(Cl)cc1C(=O)N[C@@H](Cc1ccc(Br)cc1)C(=O)OC
Reaction #1871432
3-(4-bromo-phenyl)-(2S)-[5-chloro-2-(2-methyl-butylamino)-benzoylamino]-propionic acid methyl ester
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)CNc1ccc(Cl)cc1C(=O)N[C@@H](Cc1ccc(-c2ccccc2OCc2ccccc2)cc1)C(=O)O
Reaction #1871433
title compound
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(-c2ccc(C(F)(F)F)cc2)cc1)NC(=O)c1cc(Cl)ccc1N
Reaction #2071995
2-(2-amino-5-chloro-benzoylamino)-3-(4′-trifluoromethyl-biphenyl-4-yl)-propionic acid methyl ester
Ausbeute 122.9%DOI: 10.6084/m9.figshare.5104873.v1