Issue 3, 1997

1,2-Diaminoethyl- and 1,3-diaminopropyl-derivatives of aldoses and their tautomerism

Abstract

2-Aminoethylimines and 3-aminopropylimines of aldoses have been synthesized and their structure in solutions has been investigated by 13C NMR spectroscopy. 2-Aminoethylimines usually exist as pyranoses, 3-aminopropylimines are the corresponding piperimidines while ring-ring interconversion between pyranose and piperimidine tautomers takes place in some cases.

Article information

Article type
Paper

Mendeleev Commun., 1997,7, 111-112

1,2-Diaminoethyl- and 1,3-diaminopropyl-derivatives of aldoses and their tautomerism

K. N. Zelenin, V. V. Alekseev, I. V. Ukraintsev and I. V. Tselinsky, Mendeleev Commun., 1997, 7, 111 DOI: 10.1070/MC1997v007n03ABEH000784

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