2-methyl-2-butene

O=C(O)c1cc(-c2ccc(C(F)(F)F)cc2)cs1
Reaction #9736
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCOc1ccc(CC[C@@](C)(NC(=O)OC(C)(C)C)C(=O)O)cc1
Reaction #40864
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(C(=O)O)c(OC)c1
Reaction #42141
title intermediate
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C(=O)O)c2cc([N+](=O)[O-])ccc2n1Cc1ccccc1
Reaction #44907
1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid
Rendement 101.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)N(Cc1cc(C(=O)O)cc(C(F)(F)F)c1)Cc1cc(C(F)(F)F)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45353
3-{[{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}(methoxycarbonyl)amino]methyl}-5-(trifluoromethyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1c(C)c(C#N)c2nc(C3CC3)oc2c1F
Reaction #45742
Methyl 4-cyano-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C(=O)O)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45888
4-Cyano-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-6-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1c(C2CC2)cc(C(F)(F)F)cc1C(F)(F)F
Reaction #67708
2-Cyclopropyl-4,6-bis-trifluoromethyl-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc2c(C(=O)O)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc2c(C(=O)O)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68343
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc2c(C(=O)O)c(C(C)C)n(Cc3ccccn3)c2c1
Reaction #68344
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc2c(C(=O)O)c(C(C)C)n(Cc3ncco3)c2c1
Reaction #68345
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1c(C(=O)O)c2ccc(OC)cc2n1Cc1ccccn1
Reaction #68377
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1c(I)ccn(-c2ccc(F)cc2)c1=O
Reaction #70999
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc2c(C(=O)O)c(C(C)C)n(Cc3ccccc3)c2cn1
Reaction #71543
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)O)c2cnc(Cl)cc2n1Cc1ccccc1
Reaction #71549
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1nc(C(F)(F)F)c[nH]1
Reaction #71737
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1[nH]c(C(=O)O)nc1C(F)(F)F
Reaction #71747
title compound
Rendement 118.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1[nH]c(C(=O)O)nc1C(F)(F)F
Reaction #71753
title compound
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1nc(C(=O)O)[nH]c1CC
Reaction #71767
title compound
Rendement 9.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Page 1Suivant