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296739

CCC(CC)c1cc(C(=O)OC)cc(OC)n1
Reaction #332261
2-(1-ethyl-propyl)-6-methoxy-isonicotinic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)c1cc(C(=O)O)cc(OC)n1
Reaction #332262
title compound
収率 85.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(N)=O)cc(C2CCCC2)n1
Reaction #332263
2-cyclopentyl-6-methoxy-isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NNC(=O)OCc2ccccc2)cc(C2CCCC2)n1
Reaction #332266
N′-(2-cyclopentyl-6-methoxy-pyridine-4-carbonyl)-hydrazinecarboxylic acid benzyl ester
収率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C(CC)CC)c3)n2)cc(C)c1OC[C@@H]1COC(C)(C)O1
Reaction #332282
4-{3-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-3-ethyl-5-methyl-phenyl]-[1,2,4]oxadiazol-5-yl}-2-(1-ethyl-propyl)-6-methoxy-pyridine
収率 70.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C4CCCC4)c3)n2)cc(C)c1O
Reaction #332284
4-[5-(2-cyclopentyl-6-methoxy-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol
収率 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C4CCCCC4)c3)n2)cc(C)c1OC[C@@H](O)CO
Reaction #332286
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C(CC)CC)c3)n2)cc(C)c1OC[C@@H](O)CNC(=O)CO
Reaction #332287
title compound
収率 45.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C(CC)CC)c3)n2)cc(C)c1O
Reaction #332288
2-ethyl-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenol
収率 47.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)c1cc(-c2nc(-c3cc(C)c(NS(C)(=O)=O)c(Cl)c3)no2)cc(OC)n1
Reaction #332291
title compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc(-c3cc(C)c(OC[C@@H](O)CO)c(Cl)c3)no2)cc(C2CCCC2)n1
Reaction #332292
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc(-c3cc(C)c(OC[C@@H](O)CNC(=O)CO)c(Cl)c3)no2)cc(C2CCCC2)n1
Reaction #332293
title compound
収率 57.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C(CC)CC)c3)n2)cc(C)c1NS(C)(=O)=O
Reaction #332295
title compound
収率 36.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C4CCCC4)c3)n2)cc(C)c1NS(C)(=O)=O
Reaction #332296
title compound
収率 48.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C4CCCCC4)c3)n2)cc(C)c1NS(C)(=O)=O
Reaction #332297
title compound
収率 10.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc(-c3cc(C)c(OC[C@@H](O)CO)c(Cl)c3)no2)cc(C2CCCCC2)n1
Reaction #332307
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)c1cc(C(=O)O)cc(OC)n1
Reaction #1032318
DOI: 10.1039/C8SC04228D
CCC(CC)c1cc(C(=O)OC)cc(OC)n1
Reaction #1995921
2-(1-ethyl-propyl)-6-methoxy-isonicotinic acid methyl ester
収率 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)c1cc(C(=O)O)cc(OC)n1
Reaction #1995922
title compound
収率 180.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC)nc(C2CCCC2)c1
Reaction #2365950
2-cyclopentyl-6-methoxy-isonicotinic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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