Literature DB >> 23025502

Synthesis of ynone trifluoroborates toward functionalized pyrazoles.

James D Kirkham1, Steven J Edeson, Stephen Stokes, Joseph P A Harrity.   

Abstract

The synthesis of a range of novel ynone trifluoroborates has been achieved, in a two-pot process from propargylic alcohols. These alkynes have been subsequently used in the formation of a range of pyrazole trifluoroborate salts via cyclization with hydrazines. The products are generated with high levels of regiocontrol and in excellent yields and represent versatile synthetic intermediates.

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Year:  2012        PMID: 23025502     DOI: 10.1021/ol302418b

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


  3 in total

1.  Broad Spectrum Enolate Equivalent for Catalytic Chemo-, Diastereo-, and Enantioselective Addition to N-Boc Imines.

Authors:  Barry M Trost; Chao-I Joey Hung
Journal:  J Am Chem Soc       Date:  2015-12-14       Impact factor: 15.419

2.  Metal-free synthesis of ynones from acyl chlorides and potassium alkynyltrifluoroborate salts.

Authors:  Cassandra L Taylor; Yuri Bolshan
Journal:  J Vis Exp       Date:  2015-02-24       Impact factor: 1.355

3.  Synthesis of d-glyco-alkynone derivatives via carbonylative Sonogashira reaction.

Authors:  Mariana P Darbem; C Henrique A Esteves; Isadora M de Oliveira; Joel S Reis; Daniel C Pimenta; Hélio A Stefani
Journal:  RSC Adv       Date:  2019-03-25       Impact factor: 4.036

  3 in total

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