Oxidative Halogenation of Arenes, Olefins and Alkynes Mediated by Iodine(III) Reagents

Author:

Segura-Quezada Luis A.1ORCID,Torres-Carbajal Karina R.1,Satkar Yuvraj1,Juárez Ornelas Kevin A.1,Mali Narendra1,Patil Dipak B.1ORCID,Gámez-Montaño Rocío1,Zapata-Morales Juan R.2ORCID,Lagunas-Rivera Selene1ORCID,Ortíz-Alvarado Rafael3,Solorio-Alvarado César R.1

Affiliation:

1. Departamento de Quimica, Division de Ciencias Naturales y Exactas, Universidad de Guanajuato, Noria Alta S/N, 36050 Guanajuato, Gto., Mexico

2. Departamento de Farmacia, Division de Ciencias Naturales y Exactas, Universidad de Guanajuato, Noria Alta S/N, 36050 Guanajuato, Gto., Mexico

3. Facultad de Químico Farmacobiologia. Universidad Michoacana de San Nicolas de Hidalgo, Tzintzuntzan 173, Matamoros, Morelia, Mich., Mexico

Abstract

Iodine(III)-based reagents have been broadly used in oxidative reactions for structural functionalization with several functional groups. Among the more relevant and useful synthetic transformations using these hypervalent λ3-reagents, the fluorination, chlorination, bromination, as well as the iodination protocols, can be found. Herein, we present some of the most representative oxidative halogenation procedures of arenes, olefins and alkynes dating from the oldest to the more recent advances in the area, highlighting the discovery and application of new iodine(III)-based halogenating species.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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