Stereoselective Synthesis of (–)-Heliannuol E by α-Selective Propargyl Substitution
Author:
Affiliation:
1. Department of Applied Chemistry, Meiji University
2. Organization for the Strategic Coordination of Research and Intellectual Properties, Meiji University
Abstract
Funder
Japan Society for the Promotion of Science
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0040-1719844.pdf
Reference7 articles.
1. Heliannuol E. A novel bioactive sesquiterpene of the heliannane family
2. α‐ and γ‐Regiocontrol and Enantiospecificity in the Copper‐Catalyzed Substitution Reaction of Propargylic Phosphates with Grignard Reagents
3. Asymmetric Transfer Hydrogenation of α, β-Acetylenic Ketones
4. An Ammonia-Triggered Stereocontrolled Conversion of a γ-Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D-F
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