Substructure Search

CI

CC(C)n1cc(I)nc1C1CC1
Reaction #8972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#Cc2cn(C(C)C)c(C3CC3)n2)ccn1
Reaction #8973
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(I)c2c(c1)NC(=O)CO2
Reaction #42463
title compound
Yield 91.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1C(=O)COc2c(I)cc(C(=O)OC)cc21
Reaction #42464
title compound
Yield 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2c(I)cc(C(=O)OC)cc21
Reaction #42465
title compound
Yield 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1oc2c(I)c(O)ccc2c(=O)c1-c1ccc(Cl)cc1
Reaction #42774
3-(4-Chlorophenyl)-7-hydroxy-8-iodo-2-isopropyl-chromen-4-one
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
COc1ccc(Cn2cc(I)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48600
4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Yield 71.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2cc(-c3cccc(CO)c3)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48601
4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Yield 131.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(I)c3c2CNC3=O)ccc1O[Si](C)(C)C(C)(C)C
Reaction #49475
7-iodo-4-(4-tert-butyldimethylsilyloxy-3-methoxyphenyl)isoindolinone
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(I)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50916
405
Yield 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50917
406
Yield 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2SC)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50919
409
Yield 85.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOCOc1ccc(-c2ccc(C(F)(F)F)cc2)cc1SCC(F)(F)F
Reaction #53558
(2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide
Yield 151.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1SCC(F)(F)F
Reaction #53559
2-(2,2,2-trifluoroethylthio)-4-(3-trifluoromethylpyrazolyl)benzonitrile
Yield 142.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Cl)c(SCC(F)(F)F)cc1-c1cnnn1C(F)(F)F
Reaction #53560
[2-chloro-4-fluoro-5-(3-trifluoromethyltriazolyl)phenyl] 2,2,2-trifluoroethyl sulfide
Yield 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCCCOC(=O)c1cc(I)cc(I)c1I
Reaction #56581
1-(2,3,5-triiodobenzoyloxy)-3-(z,z,z-octadeca-6,9,12-trienoyloxy)propane
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Cl)cc1I
Reaction #59677
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2cccc(N3CCOCC3)c2)cc1I
Reaction #59680
desired product
Yield 67.5%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)Cn1cc(-c2ccncc2)c(-c2ccc(OCc3ccc4ccccc4n3)cc2)n1
Reaction #62108
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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