Issue 0, 1986

Nucleophilic addition to 4,5-dihydroimidazoles: a ketone synthesis via tetrahydrofolate coenzyme models

Abstract

1-Benzyl-2-alkyl-3-methyl-4,5-dihydroimidazolium salts with Grignard reagents give addition products that are hydrolysed to ketones; 4,5-dihydroimidazoles and 4,5-dihydroimidazolium salts with hydride reagents afford N-alkylated ethane-1,2-diamines.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1986, 1995-1998

Nucleophilic addition to 4,5-dihydroimidazoles: a ketone synthesis via tetrahydrofolate coenzyme models

M. W. Anderson, R. C. F. Jones and J. Saunders, J. Chem. Soc., Perkin Trans. 1, 1986, 1995 DOI: 10.1039/P19860001995

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