Stereoselective Total Synthesis of the Nonenolide (+)-Microcarpalide
Date
2004
Authors
Banwell, Martin
Loong, David
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
The enantiomer [(+)-1] of the nonenolide natural product microcarpalide [(-)-1] has been prepared from (S)-malic acid (3) and 3-decyn-1-ol (11) via a sixteen step sequence involving, inter alia, two metathesis processes.
Description
Keywords
Keywords: malic acid; microcarpalide; natural product; nonenolide; unclassified drug; article; carbon nuclear magnetic resonance; drug synthesis; enantiomer; reaction analysis; stereochemistry
Citation
Collections
Source
Heterocycles
Type
Journal article