Busqueda de Subestructura

CCCP(c1ccccc1)c1ccccc1

O=C1c2ccccc2C(=O)N1CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #6812
3-phthalimidopropyltriphenylphosphonium bromide
Rendimiento 46.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CC/C=C\c1cccc(Cl)c1
Reaction #6813
cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide
Rendimiento 64.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(S(N)(=O)=O)s1
Reaction #7054
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C)cc1Cl
Reaction #7065
methyl 2-chloro-4-methylbenzoate
Rendimiento 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1nc2ccc(/C=C/c3ccccc3)cc2s1
Reaction #9230
desired compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(F)cc1C
Reaction #10306
title compound
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)cc2c1CCC2
Reaction #42221
6-chloro-4-methoxyindane
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(N)=O)cc(C(=O)OC)c1
Reaction #42272
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1c(O)ccc2c(=O)c(-c3ccc(Cl)cc3)c(C(C)C)oc12
Reaction #42775
8-Acetyl-3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-chromen-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)S(=O)(=O)c1ccc(C(CC3CCC(=O)C3)C(=O)Nc3ccn(C)n3)cc1N2C
Reaction #43272
Ethyl 10-methyl-8-[1-(1-methyl-1H-pyrazol-3-ylcarbamoyl)-2-(3-oxocyclopentyl)ethyl]-5,5-dioxo-5,10-dihydrophenothiazin-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Nc2ccc(C)cc2F)c(C)c(=O)n(C)c1C
Reaction #44209
desired product
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2c(C)c(=O)n(C)c3c(C)n[nH]c(=O)c23)c(F)c1
Reaction #44232
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #44397
hydrochloride salt
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(OC)c(-c2ccc(C(F)(F)F)cc2CN(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(=O)OC)c1
Reaction #45373
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncc(Cl)c1Nc1cc(=O)oc2c(OC3CCCC3)c(OC)ccc12
Reaction #48928
methyl 5-chloro-4-(8-(cyclopentyloxy)-7-methoxy-2-oxo-2H-chromen-4-ylamino)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #52353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
BrCc1cc2ccccc2o1
Reaction #57740
2-bromomethyl-benzofuran
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(C2(c3ccc(OC(F)F)cc3)N=C(N)N(C)C2=O)c1
Reaction #58865
title compound
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)=O)cc1CN(C)C
Reaction #58885
title product
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Br)cc1C(C)C
Reaction #59015
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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