Issue 8, 1985

Enantioselective synthesis of (R)- or (S)-2-alkylglutaraldehydic acid methyl esters via chiral organotin enamines

Abstract

Nucleophilic addition of chiral organotin enamines to electrophilic alkenes is described; a minor modification of experimental conditions gave the other enantiomer of 2-alkylglutaraldehydic acid methyl esters.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 504-505

Enantioselective synthesis of (R)- or (S)-2-alkylglutaraldehydic acid methyl esters via chiral organotin enamines

B. Nebout, B. de Jeso and J. Pommier, J. Chem. Soc., Chem. Commun., 1985, 504 DOI: 10.1039/C39850000504

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