carbon monoxide

O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
Reaction #3775
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(S(N)(=O)=O)s1
Reaction #7054
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(F)cn1
Reaction #8304
title compound
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc2nccc(-c3c(-c4ccccn4)nn4c3CCC4)c2c1
Reaction #8342
4-(2-Pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline-6-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cccc2[nH]c(C)cc12
Reaction #11501
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(OC(F)F)cn1
Reaction #43323
title compound
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cncc(Cl)c1Nc1cc(=O)oc2c(OC3CCCC3)c(OC)ccc12
Reaction #48928
methyl 5-chloro-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #52353
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C=Nc1ccccc1
Reaction #58789
phenylisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)c1ccc(C2(C)SC(N[C@@H](C)c3ccc(F)cc3)=NC2=O)cc1
Reaction #74420
Methyl 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ccc(C(=O)O)c2ccccc12
Reaction #78210
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)c1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #79924
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1ccc(F)c2c1C[C@@H](N(C1CCC1)C1CCC1)CO2
Reaction #80549
title compound
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCN(C1CCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80552
title compound
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1ccc(F)c2c1C[C@@H](N(C(C)C)C1CCC1)CO2
Reaction #80556
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCN(C1CCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80559
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCN(C1CCCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Reaction #80562
title compound
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1ccc(F)c2c1C[C@@H](N(C1CCCC1)C1CCC1)CO2
Reaction #80566
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)CC(C)C(=O)OC
Reaction #81643
dimethyl methylsuccinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1cc(C#N)ccc1C1C2=C(CCCC2=O)N(c2cccc(C(F)(F)F)c2)C(=O)N1C
Reaction #87934
5-Cyano-2-[3-methyl-2,5-dioxo-1-(3-trifluoromethyl-phenyl)-1,2,3,4,5,6,7,8-octahydro-quinazolin-4-yl]-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
الصفحة 1التالي