dc.contributor.author
Kennington, Stuart C. D.
dc.contributor.author
Ferré, Laura
dc.contributor.author
Romo Fernández, Juan Manuel
dc.contributor.author
Romea, Pedro
dc.contributor.author
Urpí Tubella, Fèlix
dc.contributor.author
Font Bardia, Ma. Mercedes
dc.date.issued
2019-03-04T15:22:32Z
dc.date.issued
2019-03-04T15:22:32Z
dc.date.issued
2017-06-15
dc.date.issued
2019-03-04T15:22:32Z
dc.identifier
https://hdl.handle.net/2445/129477
dc.description.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.
dc.format
application/pdf
dc.publisher
American Chemical Society
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1021/acs.joc.7b00657
dc.relation
Journal of Organic Chemistry, 2017, vol. 82, num. 12, p. 6426-6433
dc.relation
https://doi.org/10.1021/acs.joc.7b00657
dc.rights
(c) American Chemical Society , 2017
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Química Inorgànica i Orgànica)
dc.title
Diastereoselective and catalytic α-alkylation of chiral N-acyl thiazolidinethiones with stable carbocationic salts
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion