Participa en 8 reacciones

18440

O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #9710
desired compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3)nc2c1
Reaction #9712
(1R,2R)-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #59209
desired compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3)nc2c1
Reaction #59211
(1R,2R)-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #994936
desired compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3)nc2c1
Reaction #994938
(1R,2R)-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(OC(F)(F)F)cc4s3)c(F)c2)cc1
Reaction #2514577
desired compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_06
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCC[C@H]5C(=O)O)cc4)cc3)nc2c1
Reaction #2514579
(1R,2R)-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_06