A convenient formylation of 2-(Dibromomethyl)-6,11-diphenyl-5,12- naphthacenequinone using N, N -dimethylformamide or N, N -dimethylacetamide: Synthesis of 2-formyl rubrene

Synthesis

Volumn , Issue 2, 2011, Pages 287-291

  Wang, Yongfei ^a   Zhao, Hongbin ^a   Hu, Zhizhi ^a   Kimura, Masaru ^a,b   Zhiqiang, Zhang ^a   Peng, Lei ^a   Hiratsuka, Koji ^c  

^a UNIVERSITY OF SCIENCE AND TECHNOLOGY LIAONING   (China)

^b OKAYAMA UNIVERSITY   (Japan)

^c GUNMA UNIVERSITY   (Japan)

Author keywords

2 formyl rubrene; aldehyde; formylation; N, N dimethylacetamide; N, N dimethylformamide

Indexed keywords

EFFICIENT METHOD; FORMYLATION; N ,N-DIMETHYLACETAMIDE; N ,N-DIMETHYLFORMAMIDE; QUANTITATIVE YIELDS; RUBRENES; TARGET COMPOUND;

ALDEHYDES;

DIMETHYLFORMAMIDE;

2 (DIBROMOMETHYL) 6,11 DIPHENYL 5,12 NAPHTHACENEQUINONE; 2 (DIBROMOMETHYL) 6,11 DIPHENYLTETRACENE 5,12 DIONE; 2 FORMYL RUBRENE (5,6,11,12 TETRAPHENYLTETRACENE 2 CARBALDEHYDE); 5,12 DIOXO 6,11 DIPHENYL 5,12 DIHYDROTETRACENE 2 CARBALDEHYDE; CHEMICAL COMPOUND; FUNCTIONAL GROUP; N,N DIMETHYLACETAMIDE; N,N DIMETHYLFORMAMIDE; POLYCYCLIC HYDROCARBON; QUINONE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; HYDROLYSIS; SYNTHESIS;

EID: 78650970399     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258362     Document Type: Article

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