Issue 3, 1988

Asymmetric synthesis of (1R,8S)- and (1S,8S)-1-hydroxypyrrolizidin-3-ones from Boc-L-prolinal and (S)- and (R)-[(η5-C5H5)Fe(CO)(PPh3)(Ac)], respectively

Abstract

The aldol reaction between the aluminium enolate derived from (S)-[(η5-C5H5)Fe(CO)(PPh3)(Ac)](S)-(3) and Boc-L-prolinal (S)-(2) gives, after deprotection and decomplexation, (1R,8S)-1-hydroxypyrrolizidin-3-one, (1), while its epimer (1S,8S)-(1) is obtained in a similar way from (R)-(3), the inherent stereocontrol of (2) being overpowered by the iron chiral auxiliary.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 160-161

Asymmetric synthesis of (1R,8S)- and (1S,8S)-1-hydroxypyrrolizidin-3-ones from Boc-L-prolinal and (S)- and (R)-[(η5-C5H5)Fe(CO)(PPh3)(Ac)], respectively

R. P. Beckett and S. G. Davies, J. Chem. Soc., Chem. Commun., 1988, 160 DOI: 10.1039/C39880000160

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