Synthesis of new benzocyclotrimer analogues: new receptors for tetramethylammonium ion recognition

dc.contributor.author	Carrillo, Romen
dc.contributor.author	Hynes, Michael J.
dc.contributor.author	Martín, Víctor S.
dc.contributor.author	Martín, Tomás
dc.contributor.author	Crisóstomo, Fernando Pinacho
dc.date.accessioned	2018-09-20T16:02:48Z
dc.date.available	2018-09-20T16:02:48Z
dc.date.issued	2015-06-19
dc.identifier.citation	Carrillo, Romen; Hynes, Michael J. Martín, Víctor S.; Martín, Tomás; Crisóstomo, Fernando Pinacho (2015). Synthesis of new benzocyclotrimer analogues: new receptors for tetramethylammonium ion recognition. Organic Letters 17 (12), 2912-2915
dc.identifier.issn	1523-7060,1523-7052
dc.identifier.uri	http://hdl.handle.net/10379/10707
dc.description.abstract	Using a [2 + 2 + 2] cycloaddition/Mitsunobu reaction sequence, a convenient synthesis to access new benzocyclotrimer analogues has been developed. The new receptors have the geometry and functionality capable of recognizing the tetramethylammonium ion in the gas phase and in solution.
dc.publisher	American Chemical Society (ACS)
dc.relation.ispartof	Organic Letters
dc.rights	Attribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subject	constants
dc.subject	binding
dc.title	Synthesis of new benzocyclotrimer analogues: new receptors for tetramethylammonium ion recognition
dc.type	Article
dc.identifier.doi	10.1021/acs.orglett.5b01058
dc.local.publishedsource	http://doi.org/10.1021/acs.orglett.5b01058
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