Adler, P., Fadel, A., Prunet, J. and Rabasso, N. (2017) From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis. Organic and Biomolecular Chemistry, 15(2), pp. 387-395. (doi: 10.1039/c6ob02548j) (PMID:27918059)
Text
131940.pdf - Accepted Version Restricted to Repository staff only 1MB | |
Text (Supplementary information)
131940_Supp.pdf - Accepted Version Restricted to Repository staff only 10MB |
Abstract
Acyclic a-amino vinylphosphonates were alkylated through a Mitsunobu reaction then the diolefinic compounds hence formed were subjected to RCM. Studies on the scope and limitations of the RCM with these sterically hindered a-amino vinylphosphonates are detailed.
Item Type: | Articles |
---|---|
Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Prunet, Dr Joelle |
Authors: | Adler, P., Fadel, A., Prunet, J., and Rabasso, N. |
College/School: | College of Science and Engineering > School of Chemistry |
Journal Name: | Organic and Biomolecular Chemistry |
Publisher: | Royal Society of Chemistry |
ISSN: | 1477-0520 |
ISSN (Online): | 1477-0539 |
Published Online: | 05 December 2016 |
University Staff: Request a correction | Enlighten Editors: Update this record