Volume 33, Issue 6 p. 617
Cover Picture
Free Access

Cover Picture: BF3·Et2O Promoted Sulfuration of Steroidal Sapogenins (Chin. J. Chem. 6/2015)

Jun Wang

Corresponding Author

Jun Wang

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Department of Chemistry, South University of Science and Technology, Shenzhen, Guangdong 518055, China

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China, Tel.: 0086-0755-88018317; Fax: 0086-0755-88018304Search for more papers by this author
Jingjing Wu

Jingjing Wu

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Search for more papers by this author
Weisheng Tian

Corresponding Author

Weisheng Tian

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China, Tel.: 0086-0755-88018317; Fax: 0086-0755-88018304Search for more papers by this author
First published: 17 June 2015
Citations: 1

Graphical Abstract

The cover picture shows a direct synthesis of 26-thio steroidal sapogenins from natural steroidal sapogenins, which serve as an important kind of resource compounds and basic starting materials in steroidal pharmaceutical industry. This method was based on a key and magic BF3·Et2O promoted C-26 sulfuration of steroidal sapogenins, which resulted in the direct replacement of the oxygen atom in F-ring of steroidal sapogenins by sulfur. The synthesis not only provides a concise method for 26-thio steroidal sapogenins, but also presents an ideal model of the utilization of steroidal sapogenins. More details are discussed in the article by Wang and Tian et al. on page 632–636.

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