Issue 24, 1985

Benzylidene acetals of the D-ribonolactones: a structural reassessment

Abstract

The product of the reaction of D-ribono-1,4-lactone with benzaldehyde and concentrated HCl has been shown, by X-ray crystallography of its acetate, to be 3,4-O-(R)-benzylidene-D-ribono-1,5-lactone and not the 3,5-acetal as previously suggested; with ZnCl2 as catalyst the products are 2,3-O-(R)- and -(S)-benzylidene-D-ribono-1,4-lactone the former preponderating.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1826-1827

Benzylidene acetals of the D-ribonolactones: a structural reassessment

N. Baggett, J. G. Buchanan, M. Y. Fatah, C. H. Lachut, K. J. McCullough and J. M. Webber, J. Chem. Soc., Chem. Commun., 1985, 1826 DOI: 10.1039/C39850001826

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