Issue 4, 1996

Synthesis of nitrogen-containing unsaturated carbohydrates via an allyl cyanate-to-isocyanate rearrangement

Abstract

A new method for the synthesis of 4-amino-D-hex-2-enopyranosides and 2-amino-D-hex-3-enopyranosides has been developed. The key feature in this method involves construction of the allylamine moiety in the pyranose framework by employing an allyl cyanate-to-isocyanate rearrangement.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 377-382

Synthesis of nitrogen-containing unsaturated carbohydrates via an allyl cyanate-to-isocyanate rearrangement

Y. Ichikawa, C. Kobayashi and M. Isobe, J. Chem. Soc., Perkin Trans. 1, 1996, 377 DOI: 10.1039/P19960000377

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