Issue 21, 1983

Stereoselective C-alkylation of di-imine macrocycles: a versatile route to a series of meso-dialkyl-substituted macrocyclic tetramines

Abstract

Macrocycles containing two o-iminoanilino units undergo stereoselective C-alkylation on treatment with Grignard reagents or lithium alkyls to give the meso-dialkyl-substituted macrocyclic tetra-amines.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1253-1254

Stereoselective C-alkylation of di-imine macrocycles: a versatile route to a series of meso-dialkyl-substituted macrocyclic tetramines

K. Henrick, P. M. Judd, P. G. Owston, R. Peters, P. A. Tasker and R. W. Turner, J. Chem. Soc., Chem. Commun., 1983, 1253 DOI: 10.1039/C39830001253

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