Busqueda de Subestructura

175698

COc1ccc(Br)c(C(=O)O)c1OC
Reaction #6562
6-Bromo-2,3-dimethoxybenzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
OC(c1c(Br)ccc2c1OCO2)c1cccc2cnccc12
Reaction #8807
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)c(OC)c2ccccc2c1OC
Reaction #43996
ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(F)c(-c2ccccc2)c(Br)c1C#N
Reaction #45802
compound
Rendimiento 89.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cccc(Br)c1
Reaction #50379
allyl 3-bromophenyl ether
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1C=NOCCN1CCCC1)OCO2
Reaction #70964
1-(5-bromo-1,3-benzodioxol-4-yl)-N-[2-(pyrrolidin-1-yl)ethoxy]methanimine
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1-c1ccc2c(c1C=O)OCO2
Reaction #70965
5-(2-Formylphenyl)-1,3-benzodioxole-4-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(-c2ccccc2F)ccc2c1OCO2
Reaction #70966
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(-c2ccccc2Cl)ccc2c1OCO2
Reaction #70967
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(-c2ccccc2Br)ccc2c1OCO2
Reaction #70968
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2c(Br)cc(Cl)cc2O1
Reaction #80927
4-bromo-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran
Rendimiento 76.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2c(Br)ccc(N)c2O1
Reaction #80932
7-amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran
Rendimiento 83.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2c(Br)cccc2O1
Reaction #80933
4-bromo-2,3-dihydro-2,2-dimethylbenzofuran
Rendimiento 31.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2cccc(Br)c2C1=O
Reaction #80934
4-bromo-2,3-dihydro-2,2-dimethyl-3-benzofuranone
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cccc3c2C(=O)C(C)(C)O3)ccc2nc(N)nc(N)c12
Reaction #80936
2,4-diamino-5-methyl-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-4-yl)quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1c(Br)ccc2c1OCO2)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88858
title compound
Rendimiento 99.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1c(-c2ccncc2)ccc2c1OCO2)N1CCC(O)(Cc2ccccc2)CC1
Reaction #88859
title compound
Rendimiento 170.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(OC)cccc1-c1ccn[nH]1
Reaction #92489
title compound
Rendimiento 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1c(O)cccc1-c1ccc(Cl)cc1
Reaction #173157
DOI: 10.1039/C8SC04228D
CC1(C)Cc2c(Br)cc(Cl)cc2O1
Reaction #176482
DOI: 10.1039/C8SC04228D
Página 1Siguiente