Literature DB >> 26426816

A rapid and selective synthesis of α,α-fluorohalo esters via fluorohalogenative or difluorinative hydration of ynol ethers.

Liang Hu1, Chao Che, Ze Tan, Gangguo Zhu.   

Abstract

A Selectfluor-mediated fluorohalogenative or difluorinative hydration of ynol ethers is described, giving various α,α-fluorohalo esters including α,α-bromofluoro, α,α-chlorofluoro, α,α-fluoroiodo, and α,α-difluoro derivatives in a highly selective manner under very mild reaction conditions. The resultant products can be applied to the facile synthesis of α-monofluoro-α-amino acids. This reaction represents a new advance in the trifunctionalization of alkynes.

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Year:  2015        PMID: 26426816     DOI: 10.1039/c5cc07471a

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


  2 in total

1.  Chemo- and regio-divergent access to fluorinated 1-alkyl and 1-acyl triazenes from alkynyl triazenes.

Authors:  Jin-Fay Tan; Carl Thomas Bormann; Kay Severin; Nicolai Cramer
Journal:  Chem Sci       Date:  2022-02-09       Impact factor: 9.825

2.  Dihalohydration of Alkynols: A Versatile Approach to Diverse Halogenated Molecules.

Authors:  Samantha M Gibson; Jarryl M D'Oyley; Joe I Higham; Kate Sanders; Victor Laserna; Abil E Aliev; Tom D Sheppard
Journal:  European J Org Chem       Date:  2018-07-18
  2 in total

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