Issue 22, 1989

The first internally functionalized chiral [2.2]metacyclophanes

Abstract

The new medium membered heterocycles (2ci), additionally strained due to internal substituents, could be obtained after optimization of a simple one-step cyclisation reaction; the barrier of the restricted rotations of the phenyl ring in (2h) and of the t-butyl group in (2i) were measured; the X-ray, NMR, and CD data of the stable enantiomers of (2ci) are compared with those of the less strained parent skeleton (2a).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1757-1759

The first internally functionalized chiral [2.2]metacyclophanes

F. Vögtle, A. Ostrowicki, P. Knops, P. Fischer, H. Reuter and M. Jansen, J. Chem. Soc., Chem. Commun., 1989, 1757 DOI: 10.1039/C39890001757

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