Issue 14, 1970

Electrophilic substitution at C-5 in 1-methyl-5,6-dihydrocytosine

Abstract

1-Methyl-5,6-dihydrocytosine is rapidly deuteriated at C-5 at neutral pD's, treatment with iodine affords the 5-iodo-compound, and aminomethylation gives an unusual 5,5-disubstituted product (IV).

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 864-865

Electrophilic substitution at C-5 in 1-methyl-5,6-dihydrocytosine

D. M. Brown and P. F. Coe, J. Chem. Soc. D, 1970, 864 DOI: 10.1039/C29700000864

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