Highly mono-selective ortho-methylthiolation of benzamides via cobalt-catalyzed sp2 C–H activation-Reference-Cited by-同舟云学术

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Highly mono-selective ortho-methylthiolation of benzamides via cobalt-catalyzed sp2 C–H activation

Published:2018 Issue:2 Volume:5 Page:216-221
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Hu Liang¹²³⁴⁵,Chen Xiang¹²³⁴⁵,Yu Lin¹²³⁴⁵,Yu Yongqi¹²³⁴⁵,Tan Ze¹²³⁴⁵^ORCID,Zhu Gangguo⁶⁷⁸⁵^ORCID,Gui Qingwen⁹¹⁰¹¹⁵

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics

2. College of Chemistry and Chemical Engineering

3. Hunan University

4. Changsha 410082

5. P. R. China

6. Department of Chemistry

7. Zhejiang Normal University

8. Jinhua 321004

9. College of Science

10. Hunan Agricultural University

11. Changsha 410128

Abstract

A highly mono-selective ortho-methylthiolation of benzamides was achieved via Co-catalyzed coupling of benzamides with DMSO.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C7QO00717E

Reference106 articles.

2. Synthesis of thiols, selenols, sulfides, selenides, sulfoxides, selenoxides, sulfones and selenones

3. Arylthioindoles, Potent Inhibitors of Tubulin Polymerization

4. New Arylthioindoles: Potent Inhibitors of Tubulin Polymerization. 2. Structure−Activity Relationships and Molecular Modeling Studies

5. Catalytic asymmetric oxidation of aryl methyl sulfides mediated by a (S,S)-1,2-diphenylethan-1,2-diol/titanium/water complex

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