Decomplexation-nitroso Diels-Alder (NDA) approach to C,D-ring functionalisation for hippeastrine

Stephenson, G. Richard ORCID: https://orcid.org/0000-0003-1487-9178, Balfe, Andrew M., Hughes, David L. and Kelsey, Richard D. (2010) Decomplexation-nitroso Diels-Alder (NDA) approach to C,D-ring functionalisation for hippeastrine. Tetrahedron Letters, 51 (52). pp. 6806-6809. ISSN 0040-4039

Full text not available from this repository. (Request a copy)

Abstract

A tandem decomplexation-nitroso Diels-Alder (decomplexation-NDA) procedure has been shown to give the regiocontrol and stereocontrol needed for application in an organoiron-mediated synthesis of the alkaloid hippeastrine, using a selection of nitrosoarenes with functionality present to facilitate removal of the arene after the NDA step. (C) 2010 Elsevier Ltd. All rights reserved.

Item Type:	Article
Additional Information:	Stephenson, G. Richard Balfe, Andrew M. Hughes, David L. Kelsey, Richard D.
Faculty \ School:	Faculty of Science > School of Chemistry
UEA Research Groups:	Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Depositing User:	Rachel Smith
Date Deposited:	08 Jun 2011 10:45
Last Modified:	23 Oct 2022 01:40
URI:	https://ueaeprints.uea.ac.uk/id/eprint/32019
DOI:	10.1016/j.tetlet.2010.09.118

Actions (login required)

View Item