copper

O=C(O)CN(CCO)CC(=O)O
Reaction #1932
HEIDA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2044
5-(N,N-diphenylamino)acenaphthene
収率 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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
Cc1ccc(N(c2ccccc2)c2ccc3c4c(cccc24)CC3)cc1
Reaction #2049
5-[N-(4-tolyl)-N-phenylamino]acenaphthene
収率 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccc(Cl)cc3)cc2)cc1
Reaction #2421
grey-white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OC)cc(Oc2cccc(F)c2CC(=O)O)c1
Reaction #3783
2-(3,5-dimethoxyphenoxy)-6-fluorophenyl acetic acid
収率 86.1%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
COC(=O)c1ccc(-c2ccc(C(=O)OC)c(OC)c2)cc1OC
Reaction #5388
3,3'-dimethoxy-4,4'-bis(methoxycarbonyl)biphenyl
収率 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1
Reaction #6671
N,N,N′,N′-tetraphenyl-p-phenylenediamine
収率 111.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Clc1ccc2occc2c1
Reaction #7389
title compound
収率 418.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
FC(F)(F)c1ccc2nc(Cl)sc2c1
Reaction #9661
semi-solid
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1ccc(-c2sccc2-c2ccncc2)cc1
Reaction #9976
title compound
収率 109.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cccc(N(c2ccccc2)c2ccc(Nc3ccccc3)cc2)c1
Reaction #11291
N,N′-diphenyl-N-(3-tolyl)-1,4-phenylenediamine
収率 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #11800
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(N(c2ccc(OC)cc2)c2cc(Br)ccc2-c2ccc(Br)cc2)cc1
Reaction #11842
off-white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1C[C@H]2CCN(c3ccc(-c4ccc(-n5ncccc5=O)cc4)cc3)[C@H]2C1
Reaction #41232
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)CNC(=O)c1c(O)c2cc(C#N)ccc2n(C)c1=O
Reaction #41923
ethyl 2-(6-cyano-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccccc1Nc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #44466
2-[(4-Chloro-2-nitrophenyl)amino]benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C#CC(C)(C)Nc1ccc(Br)cc1
Reaction #48313
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(-n4ccnc4)ccc3OCC)nc12
Reaction #50213
title compound
収率 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
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