Issue 11, 1996

Chiral synthesis of the necic acid components, crobarbatic acid and integerrinecic acid lactone

Abstract

Samarium(II) diiodide-promoted regioselective fragmentation of the γ-halogeno esters 12 and 13 afforded the olefins 14 and 20, respectively, which were converted into the necic acid components, crobarbatic acid and a known advanced intermediate of integerrinecic acid lactone, of macropyrrolizidine alkaloids.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 1125-1130

Chiral synthesis of the necic acid components, crobarbatic acid and integerrinecic acid lactone

T. Honda, F. Ishikawa and S. Yamane, J. Chem. Soc., Perkin Trans. 1, 1996, 1125 DOI: 10.1039/P19960001125

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