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3-Chlorooxindoles: versatile starting materials for asymmetric organocatalytic synthesis of spirooxindoles
journal contributionposted on 23.07.2015 by Artur Noole, Maksim Oseka, Tonis Pehk, Mario Oeeren, Ivar Jaerving, Mark Elsegood, Andrei Malkov, Margus Lopp, Tonis Kanger
Any type of content formally published in an academic journal, usually following a peer-review process.
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.
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