A new synthesis of pteridines substituted with branched and linear alkenyl groups at C(6). The nitroso-ene reaction of 4-(alkenoylamino)-5- nitrosopyrimidines

Helvetica Chimica Acta

Volumn 90, Issue 3, 2007, Pages 521-534

  Zhang, Fang Li ^a   Schweizer, W Bernd ^a   Xu, Ming ^a   Vasella, Andrea ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CENTROSYMMETRIC DIMER; FASTER ENE REACTION; NUCLEOPHILIC ALKENOYL;

CRYSTAL STRUCTURE; DERIVATIVES; ISOMERS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

HYDROCARBONS;

2 AMINO 4 (BENZOLOXY) 6 [5 METHYL 1 METHYLIDENEHEX 4 ENYL]PTERIDIN 7 (8H) ONE; 2 AMINO 4 (BENZYLOXY) 6 [1 (TRIFLUOROMETHYL)ETHENYL]PTERIDIN 7(8H) ONE; 2 AMINO 4 (BENZYLOXY) 6 [1,5 DIMETHYLHEXA 1,4 DIENYL]PTERIDIN 7(8H) ONE; 2 AMINO 4[[ PENT 2 ENOYL]AMINO] 6 [ PROP 1 ENYL]PTERIDIN 7(8H) ONE; 2 AMINO 6 [OCT 1 ENYL] 4 (BENZYLOXY)PTERIDIN 7(8H) ONE; 2 AMINO 6 [PROP 1 ENYL] 4 (BENZYLOXY)PTERIDIN 7(8H) ONE; 2 AMINO 6 [PROP 1 ENYL]PTERIDINE 4,7(3H8H) DIONE; 2,4 BIS[[ PENT 2 ENOYL]AMINO] 6 [ PROP 1 ENYL]PTERIDIN 7(8H) ONE; 2,4 DIAMINO 6 [PROP 1 ENYL]PTERIDIN 7(8H) ONE; 4 (BENZYLOXY) 2[[(DIMETHYLAMINOA)METHYLIDENE]AMINO] 6 [ PROP 2 ENYL]PTERIDIN 7(8H) ONE; 5 NITROSO 4,6, BIS [[PENT 2 ENOYL]AMINO]PYRIMIDINE; ALKENYL GROUP; AMIDE; N (2,6 DIAMINO 5 NITROSOPYRIMIDIN 4 YL)PENT 2 ENAMIDE; N [2 AMINO 6 (BENZYLOXY) 5 NITROSOPYRIMIDIN 4 YL] 3,7 DIMETHYLOCTA 2,6 DIENAMIDE; N [2 AMINO 6 (BENZYLOXY) 5 NITROSOPYRIMIDIN 4 YL] 4,4,4 TRIFLUORO 3 METHYLBUT 2 ENAMIDE; N [2 AMINO 6 (BENZYLOXY) 5 NITROSOPYRIMIDIN 4 YL]DEC 2 ENAMIDE; N [2 AMINO 6 (BENZYLOXY) 5 NITROSOPYRIMIDIN 4 YL]PENT 2 ENAMIDE; PTERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ADDITION REACTION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; HYDROGEN BOND; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 34250642422     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200790054     Document Type: Article

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