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Issue 2, 2017
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From acyclic to cyclic α-amino vinylphosphonates by using ring-closing metathesis

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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

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Publication details

The article was received on 21 Nov 2016, accepted on 24 Nov 2016 and first published on 05 Dec 2016


Article type: Paper
DOI: 10.1039/C6OB02548J
Citation: Org. Biomol. Chem., 2017,15, 387-395
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    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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