Literature DB >> 18588347

Applications of enantioselective carbolithiation of ortho-substituted beta-methylstyrenes.

Anne-Marie L Hogan1, Thomas Tricotet, Alastair Meek, Shaista S Khokhar, Donal F O'Shea.   

Abstract

The enantioselective carbolithiation of ortho-substituted (E)-beta-methylstyrenes provides access to chiral lithiated intermediates with broad synthetic potential. Specifically, beta-methylstyrenes with o-aminomethyl, ether, and oxazoline groups have been employed in the synthesis of chiral aromatics and heteroaromatics such as isoquinolines, isoquinolinones, benzofurans, and isobenzofuranones.

Entities:  

Year:  2008        PMID: 18588347     DOI: 10.1021/jo800941h

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

Review 1.  Regio- and stereoselective intermolecular carbolithiation reactions.

Authors:  G Marsico; P Scafato; S Belviso; S Superchi
Journal:  RSC Adv       Date:  2020-09-02       Impact factor: 4.036

2.  Inter- and intramolecular enantioselective carbolithiation reactions.

Authors:  Asier Gómez-Sanjuan; Nuria Sotomayor; Esther Lete
Journal:  Beilstein J Org Chem       Date:  2013-02-13       Impact factor: 2.883

  2 in total

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