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3-Chlorooxindoles: versatile starting materials for asymmetric organocatalytic synthesis of spirooxindoles
journal contribution
posted on 2015-07-23, 09:14 authored by Artur Noole, Maksim Oseka, Tonis Pehk, Mario Oeeren, Ivar Jaerving, Mark ElsegoodMark Elsegood, Andrei MalkovAndrei Malkov, Margus Lopp, Tonis Kanger3-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.
Funding
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
History
School
- Science
Department
- Chemistry
Published in
ADVANCED SYNTHESIS & CATALYSISVolume
355Issue
5Pages
829 - 835 (7)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.Publisher
© WileyVersion
- AM (Accepted Manuscript)
Publisher statement
This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/Publication date
2013Notes
Closed accessISSN
1615-4150Publisher version
Language
- en
