Issue 38, 2005

Lewis acid-promoted reactions of zirconacyclopentadienes with isocyanates. A one-pot three-component synthesis of multiply-substituted iminocyclopentadienes from one isocyanate and two alkynes

Abstract

Multiply-substituted iminocyclopentadienes were formed from Lewis acid-promoted reactions of zirconacyclopentadienes and isocyanates via a one-pot three-component coupling process; the C[double bond, length as m-dash]O double bond of the RN[double bond, length as m-dash]C[double bond, length as m-dash]O moiety in the isocyanate was cleaved, and the isocyanates behaved formally as a one-carbon unit with Lewis acid-dependent and substituent-dependent reactions being realized.

Graphical abstract: Lewis acid-promoted reactions of zirconacyclopentadienes with isocyanates. A one-pot three-component synthesis of multiply-substituted iminocyclopentadienes from one isocyanate and two alkynes

Supplementary files

Article information

Article type
Communication
Submitted
30 Jun 2005
Accepted
02 Aug 2005
First published
05 Sep 2005

Chem. Commun., 2005, 4848-4850

Lewis acid-promoted reactions of zirconacyclopentadienes with isocyanates. A one-pot three-component synthesis of multiply-substituted iminocyclopentadienes from one isocyanate and two alkynes

J. Lu, G. Mao, W. Zhang and Z. Xi, Chem. Commun., 2005, 4848 DOI: 10.1039/B509142J

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