Functionalization of Cyclohexane Derivatives via Oxidative Radical Pathway

The straightforward functionalization of simple alkanes (simple alkanes refer particularly to cyclohexane derivatives) has been a challenging subject in modern chemistry. However, with the development of oxidative radical reaction, it provided an available and alternative approach to meet the requir...

Full description

Saved in:
Bibliographic Details
Published inChinese journal of chemistry Vol. 35; no. 3; pp. 289 - 298
Main Authors Teng, Fan, Cheng, Jiang
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag GmbH & Co. KGaA 01.03.2017
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The straightforward functionalization of simple alkanes (simple alkanes refer particularly to cyclohexane derivatives) has been a challenging subject in modern chemistry. However, with the development of oxidative radical reaction, it provided an available and alternative approach to meet the requirement of activating these compounds. In the review, we summarized the recent advances in this field, and the review mainly contained the following four parts: (1) the formation of C—C bonds; (2) the formation of C—N bonds; (3) the formation of C—S bonds and (4) the formation of C—O bonds. The straightforward functionalization of simple alkanes (simple alkanes refer particularly to cyclohexane derivatives) has been a challenging subject in modern chemistry. However, with the development of oxidative radical reaction, it provided an available and alternative approach to meet the requirement of activating these compounds. In the review, we summarized the recent advances in the field, and the review mainly contained the following four parts: (1) the formation of C—C bonds; (2) the formation of C—N bonds; (3) the formation of C—S bonds and (4) the formation of C—O bonds.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.201600538