Discovery of a multi-bond forming, four-step tandem process: construction of drug-like polycyclic scaffolds

Grafton, M.W., Farrugia, L.J., Senn, H.M. and Sutherland, A. (2012) Discovery of a multi-bond forming, four-step tandem process: construction of drug-like polycyclic scaffolds. Chemical Communications, 48, pp. 7994-7996. (doi: 10.1039/c2cc33649a)

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Publisher's URL: http://dx.doi.org/10.1039/c2cc33649a

Abstract

A one-pot tandem process involving an Overman rearrangement, ring closing enyne metathesis and a hydrogen bonding directed Diels–Alder reaction has been developed for the efficient diastereoselective synthesis of functionalised amino substituted tetralin and indene ring systems.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Farrugia, Dr Louis and Senn, Dr Hans and Sutherland, Professor Andrew
Authors: Grafton, M.W., Farrugia, L.J., Senn, H.M., and Sutherland, A.
Subjects:Q Science > QD Chemistry
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Chemical Communications
Journal Abbr.:Chem. Comm.
ISSN:1359-7345
ISSN (Online):1364-548X
Published Online:19 June 2012

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