Busqueda de Subestructura

C=Cc1ccncc1

C=Cc1ccccc1.C=Cc1ccccc1C=C.C=Cc1ccncc1
Reaction #54210
fine white solids
Rendimiento 843.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(=O)O)ccc2[nH]nc(/C=C/c3ccncc3)c12
Reaction #62324
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(=C1SCS1)c1ccncc1)c1cccc(Br)c1
Reaction #66344
1-(3-bromo-phenyl)-2-[1,3]dithietan-2-ylidene-2-pyridin-4-yl-ethanone
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(C(=Cc2ccncc2)OC2CCCCO2)c1
Reaction #66347
oil
Rendimiento 110.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)C(=C2SCS2)c2ccncc2)c1
Reaction #66360
2-[1,3]dithietan-2-ylidene-1-(3-methoxy-phenyl)-2-pyridin-4-yl-ethanone
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2n[nH]c(S)c2-c2ccncc2)c1
Reaction #66361
5-(3-methoxy-phenyl)-4-pyridin-4-yl-2H-pyrazole-3-thiol
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C(=O)C(=C2SCS2)c2ccncc2)c1
Reaction #66365
yellow solid
Rendimiento 58.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(-c2n[nH]c(S)c2-c2ccncc2)c1
Reaction #66366
3-(5-Mercapto-4-pyridin-4-yl-1H-pyrazol-3-yl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(/C=C/C(=O)O)cc(=O)n(CCN3CCC(NCc4ccc5c(c4)OCCO5)CC3)c2c1
Reaction #68042
(2E)-3-(1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-4-yl)acrylic acid
Rendimiento 77.8%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(C(=Cc2ccncc2)OC2CCCCO2)c1
Reaction #74090
oil
Rendimiento 110.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C/C=C/c1ccnc2ccccc12
Reaction #78846
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccncc2[N+](=O)[O-])=CC(O)C1
Reaction #160752
5,5-dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccncc2[N+](=O)[O-])=CC(N2C(=O)c3ccccc3C2=O)C1
Reaction #160753
2-(5,5-dimethyl-3-(3-nitropyridin-4-yl)cyclohex-2-enyl)isoindoline-1,3-dione
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2ccncc2N)=CC(N2C(=O)c3ccccc3C2=O)C1
Reaction #160754
2-(3-(3-aminopyridin-4-yl)-5,5-dimethylcyclohex-2-enyl)isoindoline-1,3-dione
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2[N+](=O)[O-])=CC(O)C1
Reaction #160758
5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enol
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1C=C(c2ccncc2N)CCC1O[Si](C)(C)C(C)(C)C
Reaction #160760
(+/−)-tert-butyl 3-(3-aminopyridin-4-yl)-6-(tert-butyldimethylsilyloxy)cyclohex-2-enylcarbamate
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1C=C(c2ccncc2[N+](=O)[O-])CCC1OS(C)(=O)=O
Reaction #160761
2-(tert-butoxycarbonylamino)-4-(3-nitropyridin-4-yl)cyclohex-3-enyl methanesulfonate
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC2C=C(c3ccncc3[N+](=O)[O-])CCC2O1
Reaction #160762
5-(3-nitropyridin-4-yl)-3,3a,7,7a-tetrahydrobenzo[d]oxazol-2(6H)-one
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=CC=C(c2ccncc2[N+](=O)[O-])C1
Reaction #160764
(+/−)-4-(5-methylcyclohexa-1,3-dienyl)-3-nitropyridine
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1cc(C2=CCN(C)CC2)ccn1
Reaction #170345
title compound
Rendimiento 17.0%DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente