部分構造検索

253110

CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(OCC(=O)OCC)CC2)c2ncnn12
Reaction #254570
DOI: 10.1039/C8SC04228D
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(O[Si](C)(C)C(C)(C)C)CC2)c2ncnn12
Reaction #606837
title compound
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n([C@H]2CC[C@H](OCC(=O)OCC)CC2)c2ncnn12
Reaction #606838
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(O[Si](C)(C)C(C)(C)C)CC2)c2ncnn12
Reaction #1499548
2-(5-{[4-(4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}pyridin-2-yl)benzonitrile
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n([C@H]2CC[C@H](OCC(=O)OCC)CC2)c2ncnn12
Reaction #1499549
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(O[Si](C)(C)C(C)(C)C)CC2)c2ncnn12
Reaction #1775804
title compound
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n([C@H]2CC[C@H](OCC(=O)OCC)CC2)c2ncnn12
Reaction #1775805
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(O[Si](C)(C)C(C)(C)C)CC2)c2ncnn12
Reaction #2135577
title compound
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n([C@H]2CC[C@H](OCC(=O)OCC)CC2)c2ncnn12
Reaction #2135578
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n(C2CCC(O[Si](C)(C)C(C)(C)C)CC2)c2ncnn12
Reaction #2149772
title compound
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(Cc2ccc(-c3ccccc3C#N)nc2)c(=O)n([C@H]2CC[C@H](OCC(=O)OCC)CC2)c2ncnn12
Reaction #2149773
title compound
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1