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Tandem allylboration-ring-closing metathesis reactions for the preparation of biologically active molecules

Authors :
P. Veeraraghavan Ramachandran
Herbert C. Brown
M. Venkat Ram Reddy
Source :
Pure and Applied Chemistry. 75:1263-1275
Publication Year :
2003
Publisher :
Walter de Gruyter GmbH, 2003.

Abstract

The development of asymmetric synthesis during the past two decades aided organic chemists considerably in the synthesis of complex natural products. Organoborane chemistry continues to play an important role in asymmetric synthesis. One of the important reactions that has become very common in the arsenal of synthetic chemists is allylboration and related reactions. Another important reaction that has recently attained enormous importance in organic chemistry is the ring-closing metathesis (RCM) reaction. Indeed, a combination of allylboration and RCM reactions provides an excellent route to cyclic ethers, lactones, lactams, etc. Herein, we describe a sequential asymmetric allylboration and RCM reaction protocol that has been utilized for the synthesis of several alpha-pyrone-containing natural products,particularly biologically active molecules.

Details

ISSN :
13653075 and 00334545
Volume :
75
Database :
OpenAIRE
Journal :
Pure and Applied Chemistry
Accession number :
edsair.doi...........cd782d32f6effea9dabb9e69b3fc9009
Full Text :
https://doi.org/10.1351/pac200375091263