From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis

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)

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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

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