Literature DB >> 30969759

Diaryl-λ3-chloranes: Versatile Synthesis and Unique Reactivity as Aryl Cation Equivalent.

Misuzu Nakajima1, Kazunori Miyamoto1, Keiichi Hirano1, Masanobu Uchiyama1,2,3.   

Abstract

We have developed a versatile, high-yield synthesis of diarylchloroniums/λ3-chloranes through the reaction of various chloroarenes with readily prepared mesityldiazonium tetrakis(pentafluorophenyl)borate under mild conditions. The scope of the reaction is broad, including ArCl, ArBr, and ArI. The diarylchloroniums/λ3-chloranes prepared here show unique reactivity in various respects, enabling intermolecular electrophilic arylation reaction of weak nucleophiles, and chlorane-halogane exchange reaction.

Entities:  

Year:  2019        PMID: 30969759     DOI: 10.1021/jacs.9b02436

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Orbital analysis of bonding in diarylhalonium salts and relevance to periodic trends in structure and reactivity.

Authors:  Shubhendu S Karandikar; Avik Bhattacharjee; Bryan E Metze; Nicole Javaly; Edward J Valente; Theresa M McCormick; David R Stuart
Journal:  Chem Sci       Date:  2022-05-19       Impact factor: 9.969

2.  Synthesis and characterization of tetraphenylammonium salts.

Authors:  Hikaru Fujita; Ozora Sasamoto; Shiori Kobayashi; Masanori Kitamura; Munetaka Kunishima
Journal:  Nat Commun       Date:  2022-05-09       Impact factor: 17.694

  2 in total

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