Issue 17, 1998

The reaction of ketene silyl acetals and silyl enol ethers with CCl4 without a promoter

Abstract

The reaction of CCl4 with ketene silyl acetals and silyl enol ethers in the absence of a promoter at ambient temperature or at reflux, or under photo-irradiation, was performed to form products via addition of the trichloromethyl group to those silyl substrates.

Article information

Article type
Paper

Chem. Commun., 1998, 1877-1878

The reaction of ketene silyl acetals and silyl enol ethers with CCl4 without a promoter

M. Mitani and H. Sakata, Chem. Commun., 1998, 1877 DOI: 10.1039/A804028A

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.

Social activity

Spotlight

Advertisements