Teilstruktursuche

C=C(C)c1cccc(C#N)c1

C=C(C)c1cccc(C#N)c1
Reaction #42360
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(CN)c1.Cl
Reaction #42361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C2=CC(O)CC2)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45871
compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C2C=CC=C2)c(N2CC[C@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45872
compound
Ausbeute 78839.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1c(C)c(C#N)c2nc(C3CC3)oc2c1F
Reaction #45886
compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1c(C)c(C#N)c2nc(C3CC3)oc2c1N1CC[C@H](N(C)C)C1
Reaction #45887
compound
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(=C2c3cc(C#N)ccc3C=Cn3cccc32)CC1
Reaction #54472
1-methyl-4-[9-cyano-11H-pyrrolo[2,1-b] [3]benzazepin-11-ylidene]piperidine
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1=C(O)C(C)(C)Oc2ccc(C#N)cc21
Reaction #64340
N-methyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)[C@H]1c2cc(C#N)ccc2OC(C)(C)[C@H]1O
Reaction #64341
cis-N-methyl-6-cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
Ausbeute 7.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C1=CC(C)(C)Oc2ccc(C#N)cc21
Reaction #64342
N-methyl-6-cyano-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2C(C(=S)Nc2ccccc2)=C1O
Reaction #64343
N-phenyl-6- cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
Ausbeute 47.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc(C#N)cc2C(C(=O)Nc2ccccc2)=C1O
Reaction #64344
N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamide
Ausbeute 21.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C)Oc2ccc(C#N)cc2C(C(=S)NC)C1O
Reaction #64345
N,2-dimethyl-6-cyano-3,4-dihydro-2-ethyl-3-hydroxy-2H-1-benzopyran-4-carbothioamide
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=S)C1=CC(C)(C)Oc2ccc(C#N)cc21
Reaction #64347
N-ethyl-6-cyano-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C)C=C(C(=O)NC)c2cc(C#N)ccc2O1
Reaction #64355
N-methyl-6-cyano-2-ethyl-2-methyl-2H-1-benzopyran-4-carboxamide
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2(CCCCc3cncn32)c2ccc(C#N)cc21
Reaction #164088
3′-Methylene-2′,3′,6,7,8,9-hexahydrospiro[imidazo[1,5-a]azepine-5,1′-indene]-5′-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(Cn1cccn1)c1cccc(C#N)c1
Reaction #177833
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2nc3cc(C#N)cc(C(C)C)c3o2)cc1
Reaction #180484
DOI: 10.1039/C8SC04228D
CN1CCC(=C2c3cc(C#N)ccc3C=Cn3cccc32)CC1
Reaction #180543
DOI: 10.1039/C8SC04228D
CN(C)CCC=C1c2cc(C=O)ccc2C=Cn2cccc21
Reaction #186725
DOI: 10.1039/C8SC04228D
Seite 1Weiter