Transition-metal-free cleavage of C–C double bonds: a three-component reaction of aromatic alkenes with S8and amides towards aryl thioamides-Reference-Cited by-同舟云学术

Transition-metal-free cleavage of C–C double bonds: a three-component reaction of aromatic alkenes with S8and amides towards aryl thioamides

Published:2018 Issue:22 Volume:5 Page:3315-3318
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Lantao¹²³⁴⁵^ORCID,Guo Zhanghong¹²³⁴⁵,Xu Kai¹²³⁴⁵,Hui Shuangshuang¹²³⁴⁵,Zhao Xiaofang¹²³⁴⁵,Wu Yangjie⁶⁷⁸⁵^ORCID

Affiliation:

1. Henan Engineering Laboratory of Green Synthesis for Pharmaceuticals

2. College of Chemistry and Chemical Engineering

3. Shangqiu Normal University

4. Shangqiu 476000

5. P. R. China

6. College of Chemistry and Molecular Engineering

7. Zhengzhou University

8. Zhengzhou 450001

Abstract

A novel transition-metal-free cleavage of C–C double bonds has been developed from a three-component reaction involving aromatic alkenes, S₈and amides, generating various aryl thioamides in up to 96% yields.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00835C

Reference59 articles.

1. Catalytic skeletal reorganization of enynes through electrophilicactivation of alkynes: double cleavage of C–C double and triple bonds

2. Oxidative Alkene Cleavage by Chemical and Enzymatic Methods

3. Chopping unfunctionalized carbon–carbon bonds: a new paradigm for the synthesis of organonitriles

4. Direct Approaches to Nitriles via Highly Efficient Nitrogenation Strategy through C–H or C–C Bond Cleavage

5. Unstrained CarbonCarbon Bond Cleavage

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