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Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Review Article

Recent Investigations on the Functionalizations of C(sp3)-H Bonds Adjacent to a Heteroatom

Author(s): Xiao-Hua Cai*, Meng-Zhi Yang and Bing Xie*

Volume 16, Issue 10, 2019

Page: [779 - 801] Pages: 23

DOI: 10.2174/1570178616666190123131353

Price: $65

Abstract

The selective functionalization of unactivated C(sp3)-H bonds has been regarded as an efficient and atom-economical approach for the formation of carbon-carbon or carbon-heteroatom bonds in modern organic synthesis. Especially, the oxidative activation of C(sp3)–H bonds adjacent to a heteroatom exhibits quite significant features in synthetic chemistry. For example, the direct functionalizations of amines, amides and ethers present important alternative tactics for the synthesis of various novel and useful molecules from simple starting materials. Many remarkable achievements in the area had continuously been made in the past decades. Here we reviewed recent investigations on the transformations of C(sp3)-H bond adjacent to a heteroatom.

Keywords: C(sp3)-H bond, functionalization, adjacent to a heteroatom, oxidative coupling, catalytic oxidative reaction, synthetic chemistry.

Graphical Abstract
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