Issue 1, 1970

Reduction of quaternary pteridines and purines by sodium borohydride

Abstract

In the 3,4-dihydro-1,3-dimethyl-5,6-diphenyl-4-oxopteridinium cation, and in the 1,3-dimethyl-8-phenylhypoxanthinium cation, position 2 of the pyrimidine ring is reduced by sodium borohydride. The analogous reaction at position 8 was observed for the 7,9-dimethylhypoxanthinium cation. The structures assigned to the reduction products are supported by u.v., i.r., and n.m.r. spectra and by degradation reactions.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 91-94

Reduction of quaternary pteridines and purines by sodium borohydride

Z. Neiman, J. Chem. Soc. C, 1970, 91 DOI: 10.1039/J39700000091

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