Literature DB >> 14602035

NaIO4-mediated selective oxidative halogenation of alkenes and aromatics using alkali metal halides.

Gajanan K Dewkar1, Srinivasarao V Narina, Arumugam Sudalai.   

Abstract

[reaction: see text] NaIO(4) oxidizes alkali metal halides efficiently in aqueous medium to halogenate alkenes and aromatics and produce the corresponding halo derivatives in excellent regio and stereoselectivity. The system also demonstrates the asymmetric version of bromo hydroxylation using beta-cyclodextrin complexes, resulting in moderate ee.

Entities:  

Year:  2003        PMID: 14602035     DOI: 10.1021/ol0358206

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


  4 in total

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Authors:  Marco Corti; Rossella Chiara; Lidia Romani; Barbara Mannucci; Lorenzo Malavasi; Paolo Quadrelli
Journal:  Photochem Photobiol Sci       Date:  2021-10-06       Impact factor: 4.328

2.  Sodium Diisopropylamide-Mediated Dehydrohalogenations: Influence of Primary- and Secondary-Shell Solvation.

Authors:  Yun Ma; Russell F Algera; Ryan A Woltornist; David B Collum
Journal:  J Org Chem       Date:  2019-08-22       Impact factor: 4.354

3.  Vinyl Thianthrenium Tetrafluoroborate: A Practical and Versatile Vinylating Reagent Made from Ethylene.

Authors:  Fabio Juliá; Jiyao Yan; Fritz Paulus; Tobias Ritter
Journal:  J Am Chem Soc       Date:  2021-08-10       Impact factor: 15.419

4.  Metalloenzyme-Inspired Ce-MOF Catalyst for Oxidative Halogenation Reactions.

Authors:  Sergio Rojas-Buzo; Patricia Concepción; José Luis Olloqui-Sariego; Manuel Moliner; Avelino Corma
Journal:  ACS Appl Mater Interfaces       Date:  2021-06-27       Impact factor: 10.383

  4 in total

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