Diastereoselective and catalytic α-alkylation of chiral N-acyl thiazolidinethiones with stable carbocationic salts

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
0022-3263
dc.identifier
https://hdl.handle.net/2445/129477
dc.identifier
672779
dc.identifier
28525716
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
8 p.
dc.format
application/pdf
dc.language
eng
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.subject
Catàlisi
dc.subject
Níquel
dc.subject
Quiralitat
dc.subject
Catalysis
dc.subject
Nickel
dc.subject
Chirality
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


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