Synlett 2004(1): 119-121  
DOI: 10.1055/s-2003-43369
LETTER
© Georg Thieme Verlag Stuttgart · New York

On the Formation of β-Hydroxy-dihydropyrroles from Metal-Catalysed Cyclisations of γ-Ynyl-β-hydroxy-α-amino Esters

David W. Knight*, Christopher M. Sharland
Cardiff School of Chemistry, Cardiff University, P.O. Box 912, Cardiff, CF10 3TB, UK
e-Mail: knightdw@cardiff.ac.uk;
Further Information

Publication History

Received 27 October 2003
Publication Date:
26 November 2003 (online)

Abstract

Copper(I), palladium(II) and mercury(II) salts in hot Et2O-pyridine mixtures can all induce 5-endo-dig cyclisations of the anti-γ-ynyl-β-hydroxy-α-amino esters 7 to give good yields of the hydroxy-dihydropyrroles 9 and subsequently the related pyrroles 8, following elimination; of the salts tested, copper(I) acetate proved to be the reagent of choice.

11

All products reported herein have been fully characterized by the usual spectroscopic and analytical data and, where possible, by comparisons with known compounds. [3] [6]