REAL

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

[img] Text
TET2012NMlacton.pdf
Restricted to Registered users only

Download (720kB)

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

Actions (login required)

Edit Item Edit Item