p-iodotoluene

Cc1ccc(Nc2ccc3c4c(cccc24)CC3)cc1
Reaction #2048
5-[N-(4-tolyl)amino]acenaphthene
収率 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1cccc(-c2ccc(C)cc2)c1
Reaction #5333
title compound
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(-c2c(Cl)cc(C(F)(F)F)cc2Cl)cc1
Reaction #53578
4-(2,6-dichloro-4-trifluoromethylphenyl)toluene
収率 85.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
c1ccc(-c2cc3ccccc3n2-c2ccccc2)cc1
Reaction #77180
1,2-diphenylindole
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1ccc(B(O)O)cc1
Reaction #77698
desired material
収率 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCOC(=O)c1ccc(C)cc1
Reaction #159272
butyl 4-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(N2c3nc(N4CCOCC4)cc(=O)n3CC[C@H]2C(F)(F)F)cc1
Reaction #167795
(8S)-9-(4-methylphenyl)-2-(morpholin-4-yl)-8-(trifluoro-methyl)-6,7,8,9-tetrahydro-4H-pyrimido[1,2-a]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(N2C(=O)CN3C(=O)CCC32)cc1
Reaction #181769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-n2cc(C)ccc2=O)cc1
Reaction #184773
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)COc1ccc(C#Cc2ccc(C)cc2)cc1
Reaction #201808
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(Oc2ccc(N3CCN(Cc4ccccc4)CC3)cc2)cc1
Reaction #201943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-n2ccc3ccccc32)cc1
Reaction #223950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCc1ccc(C#Cc2ccc(C)cc2)cc1
Reaction #225856
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-n2ccc3cc(CN4CCC(c5cccc(NC(=O)C(C)C)c5)CC4)ccc32)cc1
Reaction #230287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(N2CCN(c3c(C)c(C)c4c(c3C)CC(C)O4)CC2)cc1
Reaction #254825
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(-c2ccc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])c2)cc1
Reaction #279236
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(-n2ccc3ccc(Cl)cc32)cc1
Reaction #285962
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(N(c2ccc(C)cc2)c2ccc(Br)cc2)cc1
Reaction #352937
desired product
収率 425.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Cc1ccc(N(c2ccc(C)cc2)c2ccc(Br)cc2)cc1
Reaction #352997
desired product
収率 425.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCOC(=O)C(F)(F)c1ccc(C)cc1
Reaction #358572
title compound
収率 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
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