Literature DB >> 28548154

A biosynthetically inspired route to substituted furans using the Appel reaction: total synthesis of the furan fatty acid F5.

Robert J Lee1, Martin R Lindley, Gareth J Pritchard, Marc C Kimber.   

Abstract

Appel reaction conditions have been harnessed to affect a mild biosynthetically inspired dehydration of endoperoxides to deliver multi-substituted electron rich furans. Unlike traditional dehydrative procedures, this method is metal and acid free, and can be achieved under redox neutral conditions. It is general for a range of aryl and alkyl substituted endoperoxides, and is functional group tolerant. Furthermore, this procedure has been used to deliver an effective total synthesis of the furan fatty acid (FFA) F5.

Entities:  

Year:  2017        PMID: 28548154     DOI: 10.1039/c7cc03229c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Unified Approach to Furan Natural Products via Phosphine-Palladium Catalysis.

Authors:  Violet Yijang Chen; Ohyun Kwon
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-08       Impact factor: 15.336

2.  Discovery of four modified classes of triterpenoids delineated a metabolic cascade: compound characterization and biomimetic synthesis.

Authors:  Bin Zhou; Xin-Hua Gao; Min-Min Zhang; Cheng-Yu Zheng; Hong-Chun Liu; Jian-Min Yue
Journal:  Chem Sci       Date:  2021-06-18       Impact factor: 9.825

  2 in total

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