Issue 21, 1999

Efficient RhII binaphthol phosphate catalysts for enantioselective intramolecular tandem carbonyl ylide formation–cycloaddition of α-diazo-β-keto esters

Abstract

Catalytic enantioselective tandem carbonyl ylide formation–cycloadditions of α-diazo-β-keto ester 1 using 0.5 mol% dirhodium tetrakis(1,1′-binaphthyl-2,2′-diyl phosphate) catalysts 7–9 and 14 to give the cycloadduct 3 in good yields and up to 90% ee are described.

Supplementary files

Article information

Article type
Paper

Chem. Commun., 1999, 2185-2186

Efficient RhII binaphthol phosphate catalysts for enantioselective intramolecular tandem carbonyl ylide formation–cycloaddition of α-diazo-β-keto esters

D. M. Hodgson, P. A. Stupple and C. Johnstone, Chem. Commun., 1999, 2185 DOI: 10.1039/A906787F

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.

Social activity

Spotlight

Advertisements