A bidirectional synthesis of spiroacetals via Rh(II)-catalysed C–H insertion
No Thumbnail Available
File version
Author(s)
Lepage, Romain J
White, Jonathan M
Coster, Mark J
White, Jonathan M
Coster, Mark J
Griffith University Author(s)
Primary Supervisor
Other Supervisors
Editor(s)
Date
2017
Size
File type(s)
Location
License
Abstract
Acyclic methylene acetals bearing two diazoester subunits have been converted to [5,5]-spiroacetals VIA bidirectional C–H insertion under Rh(II) catalysis. Using a chiral Rh(II) catalyst, the major diastereomer can be produced in high enantiomeric excess (89%).
Journal Title
Chemical Communications
Conference Title
Book Title
Edition
Volume
53
Issue
30
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
Other chemical sciences not elsewhere classified