Literature DB >> 21340086

Synthesis of (1R,2R)-DPEN-derived triazolium salts and their application in asymmetric intramolecular Stetter reactions.

Min-Qiang Jia1, Yi Li, Zi-Qiang Rong, Shu-Li You.   

Abstract

A series of novel chiral triazolium salts has been synthesized from readily available (1R,2R)-DPEN and found to be efficient for the enantioselective intramolecular Stetter reaction. With 10 mol% of the catalyst, the intramolecular Stetter reaction was realized in excellent yields with up to 97% ee.

Entities:  

Year:  2011        PMID: 21340086     DOI: 10.1039/c1ob00025j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes.

Authors:  Darrin M Flanigan; Fedor Romanov-Michailidis; Nicholas A White; Tomislav Rovis
Journal:  Chem Rev       Date:  2015-05-20       Impact factor: 60.622

2.  Understanding the mechanism of the intramolecular stetter reaction. A DFT study.

Authors:  Luis R Domingo; Ramón J Zaragozá; Jose A Saéz; Manuel Arnó
Journal:  Molecules       Date:  2012-02-02       Impact factor: 4.411

3.  Enantioselective annulation of enals with 2-naphthols by triazolium salts derived from l-phenylalanine.

Authors:  Guo-Tai Li; Qing Gu; Shu-Li You
Journal:  Chem Sci       Date:  2015-04-30       Impact factor: 9.825

  3 in total

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