Electrocyclization of cis-dienals in organic synthesis: a new and versatile synthetic method for the preparation of aryl- and heteroaryl-fused coumarins

文献情報

出版日 2009-08-14

DOI 10.1039/B912887E

インパクトファクター 6.222

著者

Yung-Son Hon, Tze-Wei Tseng, Chia-Yi Cheng

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要旨

Benzo-, furo-, thieno-, and pyrido[f]coumarins were prepared by generating the 2H-pyran-2-one moieties from the oxidation of the corresponding 2H-pyran rings, which were formed in situ from the electrocyclization of cis-dienals.

掲載誌

Chemical Communications

CiteScore: 8.6

自己引用率: 4.7%

年間論文数: 2458

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

Electrocyclization of cis-dienals in organic synthesis: a new and versatile synthetic method for the preparation of aryl- and heteroaryl-fused coumarins

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