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Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates

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dc.contributor.author	De Munck, Lode
dc.contributor.author	Monleón Ventura, Alicia
dc.contributor.author	Vila Descals, Carlos
dc.contributor.author	Muñoz, M. Carmen
dc.contributor.author	Pedro, José Ramón
dc.date.accessioned	2020-03-26T15:01:44Z
dc.date.available	2020-03-26T15:01:44Z
dc.date.issued	2015
dc.identifier.citation	De Munck, Lode Monleón Ventura, Alicia Vila Descals, Carlos Muñoz, M. Carmen Pedro, José Ramón 2015 Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates Organic & Biomolecular Chemistry 13 27 7393 7396
dc.identifier.uri	https://hdl.handle.net/10550/73677
dc.description.abstract	(R)-VAPOL-Zn(II) complexes catalysed the enantioselective addition of terminal alkynes to cyclic benzoxathiazine 2,2-dioxides, providing the corresponding chiral propargylic sulfamidates with high yields (up to 93%) and good enantiomeric excesses (up to 87%).
dc.language.iso	eng
dc.relation.ispartof	Organic & Biomolecular Chemistry, 2015, vol. 13, num. 27, p. 7393-7396
dc.subject	Química orgànica
dc.subject	Catàlisi
dc.title	Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates
dc.type	journal article	es_ES
dc.date.updated	2020-03-26T15:01:45Z
dc.identifier.doi	10.1039/C5OB01012H
dc.identifier.idgrec	106685
dc.rights.accessRights	open access	es_ES