1092967-41-3Relevant academic research and scientific papers
Stereoselective total synthesis of leiocarpin C and (+)-goniodiol
Yadav,Krishna, V. Hari,Srilatha,Somaiah,Reddy, B. V. Subba
experimental part, p. 3004 - 3012 (2010/10/21)
Total syntheses of styryl lactones, leiocarpin C and (+)-goniodiol have been accomplished in a highly stereoselective manner. The key steps involved in these syntheses are the Chan alkyne reduction, Sharpless asymmetric dihydroxylation, Horner-Wadsworth-E
The first stereoselective and the total synthesis of Leiocarpin C and total synthesis of (+)-Goniodiol
Yadav,Premalatha,Harshavardhan,Subba Reddy
scheme or table, p. 6765 - 6767 (2009/04/11)
The synthesis of the styryl lactone Leiocarpin C has been achieved in a highly stereoselective manner using Jacobsen's kinetic resolution, Sharpless asymmetric epoxidation and Sharpless asymmetric dihydroxylation as key steps. This is the first total synthesis of Leiocarpin C, and thus establishes for the first time the absolute stereochemistry of this natural product.
