Literature DB >> 31247745

Synthesis of Naphthalenyl Triflates via the Cationic Annulation of Benzodiynes with Triflic Acid.

Chenxin Ge1, Guohua Wang1, Panpan Wu2,3, Chao Chen1,2,3.   

Abstract

A highly efficient and regioselective annulation of benzodiynes promoted by triflic acid has been developed. This protocol provides a step and atom-economic access to a series of naphthalenyl triflates. Furthermore, direct synthetic applications of this reaction are also elaborated through cross-coupling reactions to generate synthetically useful multisubstituted naphthalenes.

Entities:  

Year:  2019        PMID: 31247745     DOI: 10.1021/acs.orglett.9b01590

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


  2 in total

1.  Nucleophilic Addition of Enolates to 1,4-Dehydrobenzene Diradicals Derived from Enediynes: Synthesis of Functionalized Aromatics.

Authors:  Annadka Shrinidhi; Charles L Perrin
Journal:  ACS Omega       Date:  2022-06-23

2.  SuFEx-enabled, chemoselective synthesis of triflates, triflamides and triflimidates.

Authors:  Bing-Yu Li; Lauren Voets; Ruben Van Lommel; Fien Hoppenbrouwers; Mercedes Alonso; Steven H L Verhelst; Wim M De Borggraeve; Joachim Demaerel
Journal:  Chem Sci       Date:  2022-01-05       Impact factor: 9.825

  2 in total

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