Issue 13, 1993

Novel method for generation of an organotin enolate by the cleavage of diketene with bis(tributyltin) oxide, and its Michael reactions

Abstract

Generation of a novel type of organotin enolate has been accomplished by the regioselective ring cleavage of diketene with bis(tributyltin) oxide; the enolate afforded the first example of Michael addition in reactions using organotin(IV) enolates.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1067-1068

Novel method for generation of an organotin enolate by the cleavage of diketene with bis(tributyltin) oxide, and its Michael reactions

I. Shibata, M. Nishio, A. Baba and H. Matsuda, J. Chem. Soc., Chem. Commun., 1993, 1067 DOI: 10.1039/C39930001067

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements