Issue 1, 2003
From the journal:

Chemical Communications

Novel addition reactions of titanacycle phosphonates by tuning of Ti(O-i-Pr)4/2i-PrMgCl†

Abed Al Aziz Quntara  and  Morris Srebnik*a  

* Corresponding authors

a Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Hebrew University, Jerusalem, Israel
E-mail: msrebni@md.huji.ac.il
Fax: 972-2-675-7301
Tel: 972-2-675-7301

Abstract

Di- or tri-substituted vinylphosphonates, 2–5, can be obtained in a highly regio- and stereoselective manner from 1-alkynylphosphonates, by manipulation of Ti(O-i-Pr)4/2i-PrMgCl.

Graphical abstract: Novel addition reactions of titanacycle phosphonates by tuning of Ti(O-i-Pr)4/2i-PrMgCl

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Article information

DOI
https://doi.org/10.1039/B209149F
Article type
Communication
Submitted
19 Sep 2002
Accepted
13 Nov 2002
First published
25 Nov 2002

Chem. Commun., 2003, 58-59

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Novel addition reactions of titanacycle phosphonates by tuning of Ti(O-i-Pr)4/2i-PrMgCl

A. A. A. Quntar and M. Srebnik, Chem. Commun., 2003, 58 DOI: 10.1039/B209149F

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