Indium(III)-Catalyzed Reductive Bromination and Iodination of Carboxylic Acids to Alkyl Bromides and Iodides: Scope, Mechanism, and One-Pot Transformation to Alkyl Halides and Amine Derivatives-Reference-Cited by-同舟云学术

Indium(III)-Catalyzed Reductive Bromination and Iodination of Carboxylic Acids to Alkyl Bromides and Iodides: Scope, Mechanism, and One-Pot Transformation to Alkyl Halides and Amine Derivatives

Published:2013-10-23 Issue:21 Volume:78 Page:10642-10650
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Moriya Toshimitsu¹,Yoneda Shinichiro¹,Kawana Keita¹,Ikeda Reiko¹,Konakahara Takeo¹,Sakai Norio¹

Affiliation:

1. Department of Pure and Applied Chemistry, Faculty of Science and Technology, Tokyo University of Science (RIKADAI), Noda, Chiba 278-8510, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo401529j

Reference45 articles.

1. bSpargo, P. L.InComprehensive Organic Functional Group Transformations;Katritzky, A. L., Meth-Coho, O., Rees, C. W., Eds.Pergamon Press:New York, 1995; Vol.2, pp1–36.

2. Trimethylamine–borane bromide as alternative reagent for reductive bromation of aromatic carbonyl compounds

3. Reductive bromination of aromatic aldehydes using alkylboron dibromides

4. Diiodosilane. 2. A multipurpose reagent for hydrolysis and reductive iodination of ketals, acetals, ketones, and aldehydes

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