Issue 0, 1971

Syntheses of di-, tri-, and tetra-cyclopropylethylenes

Abstract

Cyclopropylethylenes have been prepared by Wittig reactions, by coupling of dicyclopropylcarbene, and by dehydration of a suitably substituted ethanol. The scope and limitations of these preparations are discussed, particularly with regard to the synthetic application of the Wittig reaction to tetrasubstituted ethylenes.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 3252-3257

Syntheses of di-, tri-, and tetra-cyclopropylethylenes

T. Teraji, I. Moritani, E. Tsuda and S. Nishida, J. Chem. Soc. C, 1971, 3252 DOI: 10.1039/J39710003252

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