Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/129477
Title: Diastereoselective and catalytic α-alkylation of chiral N-acyl thiazolidinethiones with stable carbocationic salts
Author: Kennington, Stuart C. D.
Ferré, Laura
Romo Fernández, Juan Manuel
Romea, Pedro
Urpí Tubella, Fèlix
Font Bardia, Ma. Mercedes
Keywords: Catàlisi
Níquel
Quiralitat
Catalysis
Nickel
Chirality
Issue Date: 15-Jun-2017
Publisher: American Chemical Society
Abstract: Direct nickel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commercially available nickel(II) complex, (Me3P)2NiCl2, has been developed for tropylium and trityl tetrafluoroborate salts. The reaction provides a single diastereomer of the corresponding adducts in good to high yields, which, in turn, can be easily converted into a wide array of enantiomerically pure compounds that are difficult to obtain by other asymmetric procedures.
Note: Versió postprint del document publicat a: https://doi.org/10.1021/acs.joc.7b00657
It is part of: Journal of Organic Chemistry, 2017, vol. 82, num. 12, p. 6426-6433
URI: http://hdl.handle.net/2445/129477
Related resource: https://doi.org/10.1021/acs.joc.7b00657
ISSN: 0022-3263
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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