One-pot synthesis of 1,4-diarylnaphthalenes via a Wittig-Horner reaction/[4+2] cycloaddition/dehydrogenation sequence

Synthesis

Volumn , Issue 7, 2009, Pages 1075-1080

  Chen, Zhengbo ^a   Shou, Wangge ^a   Wang, Yanguang ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

Benzyne; Cycloaddition; Diphenylnaphthalene; Tandem reaction; Wittig Horner reaction

Indexed keywords

[4 + 2] CYCLOADDITION; BENZYNE; CINNAMALDEHYDE; DIPHENYLNAPHTHALENE; ONE-POT SYNTHESIS; TANDEM PROCESS; TANDEM REACTION; WITTIG-HORNER REACTION;

ALDEHYDES; CARBOXYLATION;

SYNTHESIS (CHEMICAL);

BENZYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CINNAMALDEHYDE; NAPHTHALENE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; CHEMICAL STRUCTURE; CYCLOADDITION; DEHYDROGENATION; HORNER REACTION; ONE POT SYNTHESIS; PROCESSING; PROTON NUCLEAR MAGNETIC RESONANCE; TANDEM MASS SPECTROMETRY;

EID: 67650096278     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1083356     Document Type: Article

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