Issue 3, 1998

Practical enantiodivergent syntheses of both enantiomers of carbovir, 1592U89 and six-membered ring analogues

Abstract

The hydroxylactones 4a–b (both available in optically pure form from biocatalytic processes) have been used in the preparation of carbovir, 1592U89, and their six-membered ring analogues.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 391-392

Practical enantiodivergent syntheses of both enantiomers of carbovir, 1592U89 and six-membered ring analogues

H. F. Olivo and J. Yu, J. Chem. Soc., Perkin Trans. 1, 1998, 391 DOI: 10.1039/A708261D

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