Issue 14, 1997

Haem d1: stereoselective synthesis of the reduced form of its parent macrocycle using the original coupling strategy

Abstract

A substituted isobacteriochlorin, which corresponds structurally to the reduced metal-free macrocycle of haem d1, has been synthesised by a stereoselective route in which the final step is a photochemical 18π-electron antarafacial cyclisation of an open-chain precursor.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 2099-2110

Haem d1: stereoselective synthesis of the reduced form of its parent macrocycle using the original coupling strategy

C. J. Aucken, F. J. Leeper and A. R. Battersby, J. Chem. Soc., Perkin Trans. 1, 1997, 2099 DOI: 10.1039/A700652G

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