Issue 11, 1989

Ferrocene derivatives. Part 24. Synthesis of dihydro-2-pyrindines and dihydro-3H-2-cyclopent[c]azepines by photolysis of their cyclopentadienyliron derivatives

Abstract

Bischler-Napieralski type cyclizations of N-acyl-2-ferrocenylethylamine and N-acyl-3-ferrocenylpropylamine lead respectively to cyclopentadienyl(dihydro-2-pyrindin-5-yl)iron and cyclopentadienyl(tetrahydrocyclopent[c]azepine)iron derivatives. Photolysis of their quarternary ammonium salts liberates the metal-free azabicyclic systems.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 2075-2078

Ferrocene derivatives. Part 24. Synthesis of dihydro-2-pyrindines and dihydro-3H-2-cyclopent[c]azepines by photolysis of their cyclopentadienyliron derivatives

I. U. Khand, T. Lanez and P. L. Pauson, J. Chem. Soc., Perkin Trans. 1, 1989, 2075 DOI: 10.1039/P19890002075

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