Issue 2, 1969

4-Substituted nicotinic acids and nicotinamides. Part II. The preparation of 4-methylnicotinamide riboside

Abstract

An improved method for the synthesis of nicotinamide ribosides is described. Nicotinamide and 4-methylnicotinamide condense with 3,5-di-O-benzoly-D-ribofuranosyl chloride to give the dibenzoylribofuranosides in good yield. The ribosides obtained by mild hydrolysis contain predominantly the β-anomer.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 199-203

4-Substituted nicotinic acids and nicotinamides. Part II. The preparation of 4-methylnicotinamide riboside

M. Jarman and W. C. J. Ross, J. Chem. Soc. C, 1969, 199 DOI: 10.1039/J39690000199

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