Issue 2, 2017

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

Abstract

Acyclic α-amino vinylphosphonates were alkylated through the Mitsunobu reaction then diolefinic compounds hence formed were subjected to RCM. Studies on the scope and limitations of RCM with these sterically hindered α-amino vinylphosphonates are detailed.

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

Supplementary files

Article information

Article type
Paper
Submitted
21 Nov 2016
Accepted
24 Nov 2016
First published
05 Dec 2016

Org. Biomol. Chem., 2017,15, 387-395

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

P. Adler, A. Fadel, J. Prunet and N. Rabasso, Org. Biomol. Chem., 2017, 15, 387 DOI: 10.1039/C6OB02548J

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