iodobenzene

COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #98
Ausbeute 57.5%750 AstraZeneca ELN dataset
COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #99
Ausbeute 65.4%750 AstraZeneca ELN dataset
COC(=O)c1cc2c(ncn2C)c(F)c1Nc1ccccc1
Reaction #100
Ausbeute 75.1%750 AstraZeneca ELN dataset
COc1cccc2sc(Nc3ccccc3)nc12
Reaction #158
Ausbeute 15.2%750 AstraZeneca ELN dataset
CN(C)CCNc1ccccc1
Reaction #231
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)NCCC1CCN(c2ccccc2)CC1
Reaction #317
Ausbeute 0.0%750 AstraZeneca ELN dataset
c1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2044
5-(N,N-diphenylamino)acenaphthene
Ausbeute 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2049
5-[N-(4-tolyl)-N-phenylamino]acenaphthene
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1
Reaction #6671
N,N,N′,N′-tetraphenyl-p-phenylenediamine
Ausbeute 111.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)CCC#Cc1ccccc1
Reaction #6818
5-phenylpent-4-ynoic acid
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1ccccc1
Reaction #8521
α,α,α-trifluorotoluene
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Brc1ccc(-c2ccc(Br)cc2N(c2ccccc2)c2ccccc2)cc1
Reaction #11841
white crystals
Ausbeute 835.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCCC1COc1ccc(OCC#Cc2ccccc2)cc1
Reaction #41204
title compound
Ausbeute 17.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1CCC2N1CC(=O)N2c1ccccc1
Reaction #43389
title compound
Ausbeute 11.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1c(C)n(-c2ccccc2)c2ccc(OCc3ccccc3)cc12
Reaction #44911
5-benzyloxy-2-methyl-1-phenyl-1H-indole-3-carboxylic acid, ethyl ester
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C=C(/CC(=O)OCC)c1ccccc1
Reaction #60215
diethyl (2Z)-3-phenylpent-2-ene-1,5-dioate
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #60560
diphenylamino 4-bromobenzene
Ausbeute 161.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CSc1cccc(-c2ccccc2)c1S(=O)(=O)NC(C)(C)C
Reaction #63147
material
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
c1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #63291
triphenylamine
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1cccc(N(c2ccccc2)c2ccccc2)c1
Reaction #63292
3-methylphenyldiphenylamine
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
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