部分構造検索

OCCc1ccccc1

CCOC(=O)C=C(c1ccccc1)n1ccc2cc(OCc3ccccc3)ccc21
Reaction #52282
title compound
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52348
oil
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CN(C2CC2)C3)cc1F
Reaction #52358
title compound
収率 47.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(C)(C)O3)cc1F
Reaction #52368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2cc(C3CC3)c3c(c2)C(C)(C)CC(C)(C)O3)cc1F
Reaction #52382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1F
Reaction #52412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(O)C(=O)c1cc(OCc2ccccc2)cc2[nH]c(=O)oc12
Reaction #61654
5-benzyloxy-7-(2-ethoxy-2-hydroxy-acetyl)-3H-benzoxazol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCO)ccc2N1
Reaction #72583
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl
Reaction #74466
title compound
収率 98.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(CO)cc1C1O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1
Reaction #74508
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(c1ccc(F)c(F)c1)c1ccc(F)c(F)c1
Reaction #77451
Ethyl 3,3′,4,4′-tetrafluorobenzilate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #79915
oil
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CC(C)(C)O3)cc1F
Reaction #79937
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2cc(C3CC3)c3c(c2)C(C)(C)CC(C)(C)O3)cc1F
Reaction #79951
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(C#Cc2ccc3c(c2)C(C)(C)CCN3C2CC2)cc1F
Reaction #79981
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(O[Si](C)(C)C(C)(C)C)C(Cc1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #81134
(2RS, 3SR)-3-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-4-(4-chlorophenyl)butane
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(CC(=O)OC)cc1
Reaction #83575
4-ethinylphenylacetic acid methyl ester
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1nc(C#Cc2ccc(CC(=O)OC)cc2)ccc1O
Reaction #83576
3-{3-hydroxy-6-[2-(4-methoxycarbonylmethylphenyl)-ethinyl]-2-pyridyl}-propionic acid methyl ester
収率 39.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](C)c1ccccc1
Reaction #87980
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
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