Issue 10, 1991

Carbonyl allylation by vinyl epoxides with SnCl2–TBA or SnCl2–Lil: application to the diastereoselective synthesis of 1,3-diols

Abstract

Vinyl epoxides reacted with aldehydes in the presence of stannous chloride-tetrabutylammonium bromide or stannous chloride–lithium iodide to produce 2-vinyl-1,3-diols regio- and diastereoselectively.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 2598-2599

Carbonyl allylation by vinyl epoxides with SnCl2–TBA or SnCl2–Lil: application to the diastereoselective synthesis of 1,3-diols

Y. Masuyama, J. Nakata and Y. Kurusu, J. Chem. Soc., Perkin Trans. 1, 1991, 2598 DOI: 10.1039/P19910002598

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