Issue 16, 1993

Solvent effect and NMR behaviour in a chiral amidophosphine mediated reaction of organocuprate with chalcone

Abstract

A dramatic reversal in the direction of enantiofacial differentiation has been observed in a chiral phosphine mediated reaction of organocuprate with chalcone providing S- and R-products in diethyl ether and tetrahydrofuran (THF), respectively, and correlated with the pattern of coordination.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1248-1249

Solvent effect and NMR behaviour in a chiral amidophosphine mediated reaction of organocuprate with chalcone

M. Kanai, K. Koga and K. Tomioka, J. Chem. Soc., Chem. Commun., 1993, 1248 DOI: 10.1039/C39930001248

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