Medium Ring Ethers by Ring Expansion-Ring Contraction: Synthesis of Lauthisan.
No Thumbnail Available
File version
Author(s)
Coster, MJ
De Voss, JJ
De Voss, JJ
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
2002
Size
File type(s)
Location
License
Abstract
A new general method for the construction of medium ring ethers has been developed. This involves the ring expansion of halo-O,S-acetals followed by a Ramburg-Backlund ring contraction reaction with concomitant extrusion of the sulfur atom. This methodol. has been utilized for the synthesis of racemic cis- and trans-lauthisan (I and II resp.).
Journal Title
Organic Letters
Conference Title
Book Title
Edition
Volume
4
Issue
18
Thesis Type
Degree Program
School
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement
Item Access Status
Note
Access the data
Related item(s)
Subject
Chemical sciences