Substructure Search

25006

CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(I)cc1
Reaction #46962
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(I)cc1F
Reaction #52339
title compound
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)OCc1ccc(I)cc1
Reaction #59828
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(I)cc1F
Reaction #79904
title compound
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(I)ccc1CBr
Reaction #84355
title compound
Yield 57.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)Cc1ccc(I)cc1F
Reaction #84356
title compound
Yield 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCN1Cc1ccc(I)cc1
Reaction #163337
1-(4-Iodobenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)OCc1ccc(I)cc1
Reaction #175335
DOI: 10.1039/C8SC04228D
Ic1ccc(Cn2ccnc2)cc1
Reaction #213823
DOI: 10.1039/C8SC04228D
COC(=O)C(Oc1ccccc1)c1ccc(I)cc1
Reaction #233317
DOI: 10.1039/C8SC04228D
COC(=O)C(Oc1ccc(Cl)cc1)c1ccc(I)cc1
Reaction #233382
DOI: 10.1039/C8SC04228D
CCCc1c(OCc2ccc(I)cc2)ccc(C(C)=O)c1O
Reaction #234590
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)C(Cc1ccc(I)c(Br)c1)c1ccccc1
Reaction #239238
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(C)(C)Oc1ccc(CCC(OCc2ccc(I)cc2)c2ccc(-c3ccc(C(F)(F)F)cc3)s2)c(Cl)c1Cl
Reaction #250509
DOI: 10.1039/C8SC04228D
COC(=O)C(C)(C)OCc1ccc(I)cc1
Reaction #252868
DOI: 10.1039/C8SC04228D
CCCCc1nc(Cl)c(C=O)n1Cc1ccc(I)cc1
Reaction #289735
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccccc1)N(Cc1ccc(I)cc1)S(=O)(=O)c1c(C)cc(OC)c(C)c1C
Reaction #295206
DOI: 10.1039/C8SC04228D
Ic1ccc(CN2CCCCC2)cc1
Reaction #298008
DOI: 10.1039/C8SC04228D
O=C1CCCN1Cc1ccc(I)cc1
Reaction #317809
title compound
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cc(C(=O)OC)cc(=O)n1Cc1ccc(I)cc1F
Reaction #321946
6-Butyl-4-methoxycarbonyl-2-oxo-1-(2-fluoro-4-iodophenylmethyl)-1,2-dihydropyridine
DOI: 10.6084/m9.figshare.5104873.v1
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