2,6-dimethylpiridine

CC(C)(C)[Si](C)(C)OCC#Cc1ccccc1
Reaction #2155
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN=C(N)Nc1nc2nc(NCCCN(CC)CC)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3580
title compound
المردود 14.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Reaction #3760
diphenylmethyl ester
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Reaction #4533
liquid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC(=O)[C@H](C)Nc1ccc(F)c(F)c1F
Reaction #8524
title compound
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #42660
title compound
المردود 49.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCC(O[Si](C)(C)C(C)(C)C)c1ccc(Br)cc1
Reaction #43281
compound 5
المردود 88.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C=O)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45739
compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(CCCBr)O[Si](C)(C)C(C)(C)C
Reaction #46070
9
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC1=CC(=O)N([C@@H](CC2CCCC2)C(=O)Nc2nc(C)ns2)C1
Reaction #47230
(S)-3-cyclopentyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-N-(3-methyl-[1,2,4]thiadiazol-5-yl)-propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(O)Cn1ccc(NC(=O)C(C[C@H]2C[C@H](C)C2)N2CC(Oc3ccccc3Cl)=CC2=O)n1
Reaction #47581
2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-3-(trans-3-methyl-cyclobutyl)-propionamide
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(O)Cn1ccc(NC(=O)C(C[C@H]2C[C@@H](C)C2)N2CC(Oc3ccccc3Cl)=CC2=O)n1
Reaction #47584
2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-3-(cis-3-methyl-cyclobutyl)-propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(O)Cn1ccc(NC(=O)C(Cc2c(Cl)cccc2Cl)N2CC(Oc3c(F)cccc3F)=CC2=O)n1
Reaction #47623
3-(2,6-dichloro-phenyl)-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
المردود 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCOC[C@H](C(=O)OC(C)(C)C)[C@@H](COC(C)=O)O[Si](C)(C)C(C)(C)C
Reaction #48322
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48349
title compound
المردود 49.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)COS(=O)(=O)C(F)(F)F
Reaction #48689
desired compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(F)COS(=O)(=O)C(F)(F)F
Reaction #48701
desired compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C1CCC2=NCCCN2CC1
Reaction #49770
DBU
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1c(C)c2c(c(O)c1CC=C(C)C=CP(=O)(O)O)C(=O)OC2
Reaction #61226
[5-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-3-methyl-penta-1,3-dienyl]-phosphonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CCOCP(=O)(O)O)C(=O)OC2
Reaction #61249
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
الصفحة 1التالي