Recherche de Sous-structure

325230

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
Rendement 53.4%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
Rendement 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NC#N)C1=CC2(CCCCC2)Oc2ccc([N+](=O)[O-])cc21
Reaction #64365
N-cyano-N'-methyl-6-nitrospiro[2H-1-benzopyran-2,1'-cyclohexane]-4-carboxamidine
Rendement 73.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cccc(-c2cc(CNCCCNCCCNCC(C)C)cc(CNCCCNCCCNCC(C)C)c2)c1.Cl
Reaction #87276
desired product
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #176059
DOI: 10.1039/C8SC04228D
NS(=O)(=O)Nc1ccc2c(c1)S(=O)(=O)N=C(C1=C(O)C3C4CCC(C4)C3N(Cc3ccc(F)cc3)C1=O)N2
Reaction #189369
DOI: 10.1039/C8SC04228D
CCC1(C)C=C(C(=O)NC)c2cc(C#N)ccc2O1
Reaction #206777
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(C)NC2=C(C(=O)CNC2)C1c1cccc([N+](=O)[O-])c1
Reaction #213689
DOI: 10.1039/C8SC04228D
CNC1C=CC(C(C)C)C2CNCC12
Reaction #215710
solid
Rendement 18.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(-c2ccc(C3(F)C=CC(N4CC(CO)OC4=O)=CC3F)cn2)o1
Reaction #274153
DOI: 10.1039/C8SC04228D
CS(=O)(=O)NCc1ccc2c(c1)S(=O)(=O)N=C(C1=C(O)C3C4CCC(C4)C3N(Cc3ccc(F)cc3)C1=O)N2
Reaction #275027
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1cnc2c(c1)S(=O)(=O)N=C(C1=C(O)C3C4CCC(C4)C3N(Cc3ccc(F)cc3)C1=O)N2
Reaction #281413
DOI: 10.1039/C8SC04228D
CCSc1ccc(C(=CC2CCCC2)C(=O)Nc2ncc(F)s2)cn1
Reaction #286902
DOI: 10.1039/C8SC04228D
Cc1cc(CN2C(=O)C(C3=NS(=O)(=O)c4cc(N(C)S(C)(=O)=O)ccc4N3)=C(O)C3C4CCC(C4)C32)ccc1F
Reaction #295080
DOI: 10.1039/C8SC04228D
CCCc1c(N[C@@H](c2nnc(-c3ccc(C#N)cc3)o2)[C@H](C)O)ccc(C#N)c1Cl
Reaction #325749
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NC#N)C1=CC2(CCOCC2)Oc2ccc([N+](=O)[O-])cc21
Reaction #352027
N-cyano-N'-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-amidine
Rendement 6.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C1=CC2(CCOCC2)Oc2ccc([N+](=O)[O-])cc21
Reaction #352028
N,N-dimethyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-carboxamide
Rendement 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C1=CC2(CCSCC2)Oc2ccc([N+](=O)[O-])cc21
Reaction #352031
N-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydrothiopyran]-4-carboxamide
Rendement 33.6%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(/C(=C\C2CCCCCC2)C(=O)Nc2ncc(Br)s2)cc1
Reaction #363397
(E)-N-(5-bromo-thiazol-2-yl)-3-cycloheptyl-2-(4-methanesulfonyl-phenyl)-acrylamide
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.N#CC1(Cl)CC2C=CC1NC2
Reaction #367052
7-Chloro-7-cyano-2-azabicyclo[2.2.2]oct-5-ene hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1
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