部分構造検索

14771

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.v1
N#Cc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9432
desired product
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cccc(C#N)c1
Reaction #42360
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(C#N)c3)cc2C1
Reaction #46705
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(F)c(C#N)c2)CC1
Reaction #48150
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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
収率 3.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)C1=Cc2ccc(-c3cccc(C#N)c3)cc2N=C(N)C1
Reaction #66287
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccnc(Cl)n2)cc(N2CCOCC2)c1
Reaction #69024
3-(2-Chloropyrimidin-4-yl)-5-morpholinobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccnc3[nH]ccc23)cc1-c1cccc(C#N)c1
Reaction #69155
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
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
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccnc3[nH]ccc23)cc1-c1cccc(C#N)c1
Reaction #73186
product
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
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
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(B(O)O)c1
Reaction #77592
title compound
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(Cl)c2)OC1(C)C
Reaction #79854
title compound
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(F)c2)OC1(C)C
Reaction #79857
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(B2OC(C)(C)C(C)(C)O2)ccc1Oc1ccccc1
Reaction #79860
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c([N+](=O)[O-])c2)OC1(C)C
Reaction #79864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(C=O)c2)OC1(C)C
Reaction #79867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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