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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/18310

Title: 3-Chlorooxindoles: versatile starting materials for asymmetric organocatalytic synthesis of spirooxindoles
Authors: Noole, Artur
Oseka, Maksim
Pehk, Tonis
Oeeren, Mario
Jaerving, Ivar
Elsegood, Mark R.J.
Malkov, Andrei V.
Lopp, Margus
Kanger, Tonis
Keywords: Asymmetric synthesis
Spiro compounds
Issue Date: 2013
Publisher: © Wiley
Citation: NOOLE, A. et al., 2013. 3-Chlorooxindoles: versatile starting materials for asymmetric organocatalytic synthesis of spirooxindoles. Advanced Synthesis and Catalysis, 355 (5), pp. 829 - 835.
Abstract: 3-Chlorooxoindoles have emerged as versatile precursors in the synthesis of spirocyclopropyl oxindoles. High enantio- and diastereoselectivity was attained under conditions of both iminium/enamine and H-bonding catalysis.
Description: Closed access
Sponsor: Estonian Science Foundation. Grant Number: grants no. 8289 and 8880 Ministry of Education and Research. Grant Number: 0140060s12 EU European Regional Development Fund. Grant Number: 3.2.0101.08-0017 COST-ORCA action. Grant Number: CM0905
Version: Accepted for publication
DOI: 10.1002/adsc.201300019
URI: https://dspace.lboro.ac.uk/2134/18310
Publisher Link: http://dx.doi.org/10.1002/adsc.201300019
ISSN: 1615-4150
Appears in Collections:Closed Access (Chemistry)

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