An expedient asymmetric synthesis of a calystegine B4 analogue

dc.contributor.author	Koulocheri, SD	en
dc.contributor.author	Pitsinos, EN	en
dc.contributor.author	Haroutounian, SA	en
dc.date.accessioned	2014-06-06T06:44:59Z
dc.date.available	2014-06-06T06:44:59Z
dc.date.issued	2002	en
dc.identifier.issn	00397881	en
dc.identifier.uri	http://62.217.125.90/xmlui/handle/123456789/2191
dc.relation.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-0346037051&partnerID=40&md5=70b1692b147f5afc2b668d0bdd604cb4	en
dc.subject	Alkaloids	en
dc.subject	Asymmetric synthesis	en
dc.subject	Calystegines	en
dc.subject	Glycosidase inhibitors	en
dc.subject	Piperidines	en
dc.subject.other	Hydroxylation	en
dc.subject.other	Polyhydroxylation	en
dc.subject.other	Synthesis (chemical)	en
dc.subject.other	alkaloid derivative	en
dc.subject.other	calystegine B4	en
dc.subject.other	glycosidase inhibitor	en
dc.subject.other	tropane derivative	en
dc.subject.other	unclassified drug	en
dc.subject.other	article	en
dc.subject.other	asymmetric synthesis	en
dc.subject.other	chemical analysis	en
dc.subject.other	chemical bond	en
dc.subject.other	chemical reaction	en
dc.subject.other	diastereoisomer	en
dc.subject.other	drug structure	en
dc.subject.other	drug synthesis	en
dc.subject.other	high performance liquid chromatography	en
dc.subject.other	proton nuclear magnetic resonance	en
dc.subject.other	reduction	en
dc.subject.other	stereochemistry	en
dc.subject.other	technique	en
dc.title	An expedient asymmetric synthesis of a calystegine B4 analogue	en
heal.type	journalArticle	en
heal.publicationDate	2002	en
heal.abstract	A convenient high-yielding synthetic route to polyhydroxylated 6-oxa-nor-tropanes that mimic the structural framework of calystegine B4 is reported.	en
heal.journalName	Synthesis	en
dc.identifier.issue	12	en
dc.identifier.spage	1707	en
dc.identifier.epage	1710	en