Literature DB >> 25162482

Hypervalent iodine(III)-mediated oxidative decarboxylation of β,γ-unsaturated carboxylic acids.

Kensuke Kiyokawa1, Shunsuke Yahata, Takumi Kojima, Satoshi Minakata.   

Abstract

A novel oxidative decarboxylation of β,γ-unsaturated carboxylic acids mediated by hypervalent iodine(III) reagents is described. The decarboxylative C-O bond forming reaction proceeded in the presence of PhI(OAc)2 to give the corresponding allylic acetates. In addition, decarboxylative C-N bond formation was achieved by utilizing hypervalent iodine(III) reagents containing an I-N bond. Mechanistic studies suggest the unique reactivity of hypervalent iodine reagents in this ionic oxidative decarboxylation.

Entities:  

Year:  2014        PMID: 25162482     DOI: 10.1021/ol5022433

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


  4 in total

1.  Direct Decarboxylative Functionalization of Carboxylic Acids via O-H Hydrogen Atom Transfer.

Authors:  Christina G Na; Davide Ravelli; Erik J Alexanian
Journal:  J Am Chem Soc       Date:  2019-12-26       Impact factor: 15.419

2.  Hypervalent iodine(III)-mediated decarboxylative acetoxylation at tertiary and benzylic carbon centers.

Authors:  Kensuke Kiyokawa; Daichi Okumatsu; Satoshi Minakata
Journal:  Beilstein J Org Chem       Date:  2018-05-15       Impact factor: 2.883

3.  Umpolung carbonyls enable direct allylation and olefination of carbohydrates.

Authors:  Jian Kan; Zhangpei Chen; Zihang Qiu; Leiyang Lv; Chenchen Li; Chao-Jun Li
Journal:  Sci Adv       Date:  2022-03-09       Impact factor: 14.136

4.  Sterically Congested 2,6-Disubstituted Anilines from Direct C-N Bond Formation at an Iodine(III) Center.

Authors:  Nicola Lucchetti; Michelangelo Scalone; Serena Fantasia; Kilian Muñiz
Journal:  Angew Chem Int Ed Engl       Date:  2016-10-10       Impact factor: 15.336

  4 in total

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