dichloropalladium

COc1ccc(CCCCCCCCOc2ccc(CO)nc2C=CC(=O)O)cc1
Reaction #1849
3-{6-Hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=C(C(=O)OCC)c1nc(C)ccc1O
Reaction #1850
Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C=CC(=O)O)cc1
Reaction #2452
p-methoxy cinnamic acid
収率 81.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cnc2nc(N)nc(N)c2c1
Reaction #4541
2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbonitrile
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NS(=O)(=O)c1ccccc1
Reaction #4835
phenylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCc1cc(OCc2ccc(-c3ccccc3C#N)cc2)c2ccccc2n1
Reaction #5776
4'-[(2-ethylquinolin-4-yloxy)methyl]biphenyl-2-carbonitrile
収率 91.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)Nc1cc2c(O)n(C#CCOC3CCCCO3)cnc-2n1
Reaction #6623
3-(3-tetrahydropyr-2-yloxyprop-1-yn-1-yl)-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)C(=O)Nc1cc2c(O)n(C#C[Si](C)(C)C)cnc-2n1
Reaction #6626
3-trimethylsilylethynyl-4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CC(Cc2ccccc2)CO1
Reaction #8291
title compound
収率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1ccc(F)cn1
Reaction #8304
title compound
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1cc(F)cc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9433
desired product
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)[C@H](C(=O)O)C(C)C
Reaction #40873
Valsartan
収率 55.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCCC1COc1ccc(OCC#Cc2ccccc2)cc1
Reaction #41204
title compound
収率 17.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCCC1COc1ccc(OCC#Cc2ccc(CO)cc2)cc1
Reaction #41205
title compound
収率 20.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCCC1COc1ccc(OCC#Cc2ccc(Br)cc2)cc1
Reaction #41206
title compound
収率 33.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ccccc2)cc1
Reaction #42150
4-methylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(-c2ccccc2)cc1
Reaction #42168
4-methylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)Nc1cccc(CCC=O)c1
Reaction #44177
title compound
収率 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(/C=C/C(=O)O)cn1
Reaction #46488
title compound
収率 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc([C@@]2(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1Cc1ccc(OC(F)(F)F)cc1
Reaction #48112
4-(β-D-glucopyranos-1-yl)-2-(4-trifluoromethoxy-benzyl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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