Sulfur-containing dihydro-pyrrolo [60]fullerene derivatives via 1,3-dipolar cycloadditions of glycine imine esters to C 60

dc.contributor.author	Ioannou, E	en
dc.contributor.author	Hirsch, A	en
dc.contributor.author	Elemes, Y	en
dc.date.accessioned	2014-06-06T06:47:33Z
dc.date.available	2014-06-06T06:47:33Z
dc.date.issued	2007	en
dc.identifier.uri	http://dx.doi.org/10.1016/j.tet.2007.05.011	en
dc.identifier.uri	http://62.217.125.90/xmlui/handle/123456789/3679
dc.subject	Mass Spectrometry	en
dc.subject	uv-vis spectroscopy	en
dc.title	Sulfur-containing dihydro-pyrrolo [60]fullerene derivatives via 1,3-dipolar cycloadditions of glycine imine esters to C 60	en
heal.type	journalArticle	en
heal.identifier.primary	10.1016/j.tet.2007.05.011	en
heal.publicationDate	2007	en
heal.abstract	C60 reacts thermally with 1,3-dipoles, formed in situ, from sulfide-bearing imines of glycine esters, and affords dihydro-pyrrolo [60]fullerene derivatives containing a vinylic sulfide group, which were isolated in good yields, and characterized with 1H and 13C NMR, FTIR, UV–vis spectroscopies, and with FAB, ESI mass spectrometries. The new derivatives contain a sulfide, an imine, and an ester functionality for further	en
heal.journalName	Tetrahedron	en
dc.identifier.doi	10.1016/j.tet.2007.05.011	en