Busqueda de Subestructura

10557

O=C(O)c1ccc(OC2CCCCO2)cc1
Reaction #7427
p-tetrahydropyranyloxy benzoic acid
Rendimiento 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(OC(=O)c1ccc(OCc2ccccc2)cc1)C(F)(F)F
Reaction #49701
titled compound
Rendimiento 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC[C@@H](OC(=O)c1ccc(OCc2ccccc2)cc1)C(F)(F)F
Reaction #49705
titled compound
Rendimiento 61.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCOc1ccc(C(=O)CCC(=O)O)cc1)Cc1ccccc1F
Reaction #53288
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)Nc2ccccc2NCC2CCN(c3ccncc3)CC2)cc1
Reaction #78116
title compound
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)Nc2cnccc2NCC2CCN(c3ccncc3)CC2)cc1
Reaction #78126
title compound
Rendimiento 6.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNC(=O)c1ccc(OCc2ccccc2)cc1
Reaction #81360
N-(4-(phenylmethoxy)benzoyl)glycine
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1ccc(OCc2ccccc2)cc1)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #81361
N-(4-(phenylmethoxy)benzoyl)glycine pentafluorophenyl ester
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCCCN2CCC(c3noc4cc(F)ccc34)CC2)c(C)c1.CC(=O)c1ccc(OCCCN2CCC(c3noc4cc(F)ccc34)CC2)c(C)c1.O=C(O)/C=C/C(=O)O
Reaction #83859
1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methylphenyl]-ethanone hemifumarate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(C)(C)c1[nH]c3c(N)c(C#N)ccc3c1C2=O
Reaction #90133
title compound
Rendimiento 27.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Oc2ccccc2)cc1
Reaction #158104
4-Phenoxybenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158118
solid
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Oc2ccccc2)cc1
Reaction #158119
4-Phenoxybenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158122
solid
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Oc2ccccc2)cc1
Reaction #158123
4-Phenoxybenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158125
solid
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(Oc2ccccc2)cc1
Reaction #158126
4-Phenoxybenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158154
solid
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C2CC3CC1CN(C3)C2)c1ccc(Oc2ccccc2)cc1
Reaction #174499
DOI: 10.1039/C8SC04228D
CCCCOc1ccc(C(=O)NC2CCc3c(O)ccc(N4CCN(C)CC4)c3C2)cc1
Reaction #175718
DOI: 10.1039/C8SC04228D
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