Issue 0, 1982

The chemistry of organoborates. Part 8. Unique Michael reactions of lithium trialkylalkynylborates

Abstract

Lithium trialkylalkynylborates undergo unique Michael reactions involving migration of an alkyl group from boron to carbon. Oxidation or hydrolysis of the vinylboranes so produced yields compounds of synthetic potential. The generality and limitations of the Michael reactions are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 719-722

The chemistry of organoborates. Part 8. Unique Michael reactions of lithium trialkylalkynylborates

A. Pelter, L. Hughes and J. M. Rao, J. Chem. Soc., Perkin Trans. 1, 1982, 719 DOI: 10.1039/P19820000719

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