Issue 12, 2004

A novel asymmetric route to succinimides and derived compounds: synthesis of the lignan lactone (+)-hinokinin

Abstract

A novel approach to chiral succinimides and derived compounds has been developed that involves chiral lithium amide desymmetrisation of an N-ortho-tert-butylphenyl succinimide to generate a putative atropisomeric intermediate enolate, alkylation of which enables access to the lignan lactone (+)-hinokinin.

Graphical abstract: A novel asymmetric route to succinimides and derived compounds: synthesis of the lignan lactone (+)-hinokinin

Article information

Article type
Communication
Submitted
03 Mar 2004
Accepted
19 Apr 2004
First published
14 May 2004

Chem. Commun., 2004, 1392-1393

A novel asymmetric route to succinimides and derived compounds: synthesis of the lignan lactone (+)-hinokinin

D. J. Bennett, P. L. Pickering and N. S. Simpkins, Chem. Commun., 2004, 1392 DOI: 10.1039/B403193H

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