University of Surrey

Test tubes in the lab Research in the ATI Dance Research

Silenes as novel synthetic reagents: synthesis of diols and lactones from simple alkyldienes

Berry, MB, Griffiths, RJ, Sanganee, MJ, Steel, PG and Whelligan, DK (2003) Silenes as novel synthetic reagents: synthesis of diols and lactones from simple alkyldienes Tetrahedron Lett, 44 (51). pp. 9135-9138.

Full text not available from this repository.

Abstract

Aryl substituted silenes can be generated by a modified Peterson olefination reaction and trapped in situ to afford silacycles with high diastereoselectivity. These silacycles can be elaborated by 'Fleming-Tamao' type oxidation to provide access to functionalized diols and lactones. (C) 2003 Elsevier Ltd. All rights reserved.

Item Type: Article
Authors :
NameEmailORCID
Berry, MBUNSPECIFIEDUNSPECIFIED
Griffiths, RJUNSPECIFIEDUNSPECIFIED
Sanganee, MJUNSPECIFIEDUNSPECIFIED
Steel, PGUNSPECIFIEDUNSPECIFIED
Whelligan, DKd.whelligan@surrey.ac.ukUNSPECIFIED
Date : 15 December 2003
Identification Number : https://doi.org/10.1016/j.tetlet.2003.10.056
Uncontrolled Keywords : silene, Diels-Alder cycloaddition, silacycles, Fleming-Tamao oxidation, diols, lactones, SILICON-CARBON HETEROCYCLES, ORGANIC-SYNTHESIS, BOND, CONVERSION, SILACYCLES, OXIDATION
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 12:07
Last Modified : 17 May 2017 15:01
URI: http://epubs.surrey.ac.uk/id/eprint/834109

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year


Information about this web site

© The University of Surrey, Guildford, Surrey, GU2 7XH, United Kingdom.
+44 (0)1483 300800