Literature DB >> 11101428

A novel synthesis of 4H-chromen-4-ones via intramolecular wittig reaction

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Abstract

The acylphosphoranes formed in a sequential manner from the reaction of the silyl ester of O-acyl(aroyl)salicylic acids and (trimethylsilyl)methylenetriphenylphosphorane undergo intramolecular Wittig cyclization on the ester carbonyl to afford the 4H-chromen-4-ones in good to excellent yields.

Entities:  

Year:  2000        PMID: 11101428     DOI: 10.1021/ol006518p

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  A mild and efficient method for the synthesis of a new class of furo[3,2-c]chromenes in aqueous media.

Authors:  Mohammad A Khalilzadeh; Zinatossadat Hossaini; Faramarz Rostami Charati; Sara Hallajian; Mehdi Rajabi
Journal:  Mol Divers       Date:  2010-08-25       Impact factor: 2.943

2.  A novel one-pot synthesis of flavones.

Authors:  Meng-Yang Chang; Min-Chen Tsai; Chun-Yi Lin
Journal:  RSC Adv       Date:  2021-03-22       Impact factor: 3.361

  2 in total

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