3-cyano-phenylboronic acid

Cc1ccc(-c2nc3ccccc3o2)cc1-c1cccc(C#N)c1
Reaction #7785
5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9432
desired product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C(C)c1cccc(C#N)c1
Reaction #42360
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(C#N)c3)cc2C1
Reaction #46705
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2cccc(C#N)c2)CC1
Reaction #48142
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cccc(C#N)c3)c2c1
Reaction #53703
N-[3-(3-cyanophenyl)-1 H-indazol-5-yl]-2-methylsulfonylbenzenesulfonamide
Ausbeute 3.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCN(CCC)C(=O)C1=Cc2ccc(-c3cccc(C#N)c3)cc2N=C(N)C1
Reaction #66287
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1=Cc2ccc(-c3cccc(C#N)c3)cc2N=C(NC(=O)OC(C)(C)C)C1
Reaction #66291
(1E,4E)-ethyl 2-(tert-butoxycarbonylamino)-8-(3-cyanophenyl)-3H-benzo[b]azepine-4-carboxylate
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nn(-c2ccnc3[nH]ccc23)cc1-c1cccc(C#N)c1
Reaction #69155
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[Si](C)(C)CCOCn1ccc2c(-c3cnn(-c4cccc(C#N)c4)c3)ccnc21
Reaction #69214
3-[4-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]-benzonitrile
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1nn(-c2ccnc3[nH]ccc23)cc1-c1cccc(C#N)c1
Reaction #73186
product
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[Si](C)(C)CCOCn1ccc2c(-c3cnn(-c4cccc(C#N)c4)c3)ccnc21
Reaction #73248
3-[4-(1-[2-(trimethylsilyl)ethoxy]methyl-1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-1-yl]-benzonitrile
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(Cc1ccc(OCC(=O)OC(C)(C)C)c(-c2cccc(C#N)c2)c1)S(=O)(=O)c1ccc(F)cc1
Reaction #155769
t-butyl 2-(2-(3-cyanophenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetate
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)COc1ccc(CNS(=O)(=O)c2ccc(F)cc2)cc1-c1cccc(C#N)c1
Reaction #155773
t-butyl 2-(2-(3-cyanophenyl)-4-((4-fluorophenylsulfonamido)methyl)phenoxy)acetate
Ausbeute 76.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1cc(-c2ccc3ncc(Cc4ccc5ncc(-c6cccc(C#N)c6)n5c4)n3n2)cn1
Reaction #156484
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)CCC(N(CCOc2ccc(-c3cccc(C#N)c3)cc2)C(=O)OC(C)(C)C)CC1
Reaction #157490
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1OCC(C)(c2cccc(-c3cccc(C#N)c3)c2)NC1=N
Reaction #160457
5-(3-(3-cyanophenyl)phenyl)-2,5-dimethyl-1,2,4-oxadiazinan-3-imine
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1cccc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)c1
Reaction #167627
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)N(C)CC(=O)N(Cc2ccc(-c3cccc(C#N)c3)cc2)c2ccc(C(=O)OCc3ccccc3)c(OCc3ccccc3)c2)cc1
Reaction #169050
29
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C(=O)c1cc2c(s1)-c1ccc(-c3cccc(C#N)c3)cc1OCC2)c1ccccc1Cl
Reaction #171684
199
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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