Issue 11, 1986

The chemistry of spiroacetals. An enantiospecific synthesis of the spiroacetal moiety of milbemycins α7 and α8

Abstract

An enantiospecific synthesis of the dioxygenated spiroacetal moiety of milbemycins α7 and α8 has been developed from the appropriate epoxide and regioselective acylation of the C-23 alcohol.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 874-876

The chemistry of spiroacetals. An enantiospecific synthesis of the spiroacetal moiety of milbemycins α7 and α8

R. Baker, C. J. Swain and J. C. Head, J. Chem. Soc., Chem. Commun., 1986, 874 DOI: 10.1039/C39860000874

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