Literature DB >> 26551928

Synergistic Acid-Promoted Synthesis of Highly Substituted Butenolides via the Annulation of Keto Acids and Tertiary Alcohols.

Wenbin Mao1, Chen Zhu1,2.   

Abstract

An efficient and practical approach to highly substituted butenolides via the annulation of keto acids and tertiary alcohols is described. The synergistic effect provided by the combination of Lewis and Brønsted acids is crucial to the reaction outcome. A variety of highly substituted butenolides are readily produced in synthetically useful yields. Water is the only waste from the reaction, therefore making it an environmentally benign and atom-economical process for butenolide synthesis.

Entities:  

Year:  2015        PMID: 26551928     DOI: 10.1021/acs.orglett.5b03026

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


  1 in total

1.  BF3·Et2O-Mediated annulation of α-keto acids with aliphatic ketones for the synthesis of γ-hydroxy-butenolides and γ-alkylidene-butenolides.

Authors:  Zhenfeng Cheng; Qingyun Gu; Yushan Xie; Yanan Zhang; Xiaobao Zeng
Journal:  RSC Adv       Date:  2022-08-25       Impact factor: 4.036

  1 in total

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