Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized b-aminocyclohexanecarboxylate stereoisomers

Nonn, Melinda and Kiss, Loránd and Sillanpää, Reijo and Fülöp, Ferenc (2012) Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized b-aminocyclohexanecarboxylate stereoisomers. Tetrahedron, 68. pp. 9942-9948. ISSN 0040-4020

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Official URL: http://dx.doi.org/10.1016/j.tet.2012.09.085

Abstract

Highly functionalized b-aminocyclohexanecarboxylate regio- and stereoisomers were synthesized from a bicyclic b-lactam by successive regioselective iodolactonization, stereo- and regioselective nitrile oxide cycloaddition, lactone ring-opening and isoxazoline ring-opening

Item Type:	Article
Subjects:	Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia
Depositing User:	Dr Loránd Kiss
Date Deposited:	30 Dec 2015 19:47
Last Modified:	30 Dec 2015 19:47
URI:	http://real.mtak.hu/id/eprint/31590

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