4-Alkenyl-5H-1, 2, 3-oxathiazole 2, 2-dioxides in catalytic and enantioselective [4 + 2] cycloaddition through iminium activation. Straightforward access to the trans-decaline framework and to densely functionalized cyclohexanes1. Issue 3 (17th March 2015)

• Record Type: Journal Article
• Authors: Riaño, Iker; Uria, Uxue; Carrillo, Luisa; Reyes, Efraim; Vicario, Jose L.
• Is Part Of: Organic chemistry frontiers. Volume 2:Issue 3(2015:Mar.)
• Page Start: 206
• Page End: 210
• Publication Date: 2015-03-17
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/c4qo00316k
• Languages: English
• ISSNs: 2052-4110

Abstract

<abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgj40zm0kf" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />4-Alkenyl-5<italic>H</italic>-1, 2, 3-oxathiazole 2, 2-dioxides undergo Michael/Michael cascade reaction with enals through iminium/enamine activation.</p> </abstract>