Synthetic studies towards trichodimerol and related vertinoid polyketides: Preliminary communication

dc.contributor.author	Pitsinos, EN	en
dc.contributor.author	Vidali, VP	en
dc.contributor.author	Couladouros, EA	en
dc.date.accessioned	2014-06-06T06:45:09Z
dc.date.available	2014-06-06T06:45:09Z
dc.date.issued	2002	en
dc.identifier.issn	14246376	en
dc.identifier.uri	http://62.217.125.90/xmlui/handle/123456789/2276
dc.relation.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-3242663232&partnerID=40&md5=a719ce828194803feff5ead4b4f5f82b	en
dc.subject	Asymmetric reduction	en
dc.subject	Epoxysorbicillinol	en
dc.subject	Quinoles	en
dc.subject	Quinones	en
dc.subject.other	bisorbicillinol	en
dc.subject.other	epoxysorbicillinol	en
dc.subject.other	penicillin derivative	en
dc.subject.other	polyketide	en
dc.subject.other	trichodimerol	en
dc.subject.other	unclassified drug	en
dc.subject.other	article	en
dc.subject.other	Diels Alder reaction	en
dc.subject.other	dimerization	en
dc.subject.other	drug structure	en
dc.subject.other	drug synthesis	en
dc.subject.other	enantioselectivity	en
dc.subject.other	Michael addition	en
dc.subject.other	oxidation	en
dc.title	Synthetic studies towards trichodimerol and related vertinoid polyketides: Preliminary communication	en
heal.type	journalArticle	en
heal.publicationDate	2002	en
heal.abstract	An alternative synthetic route towards trichodimerol, bisorbicillinol and epoxysorbicillinol employing a suitable para-quinol as a common versatile key synthetic intermediate was investigated. The validity of this approach for the preparation of bisorbicillinol and epoxy-sorbicillinol derivatives was demonstrated. However, attempts to obtain trichodimerol-related derivatives or to render this approach enantioselective were unsuccessful.	en
heal.journalName	Arkivoc	en
dc.identifier.issue	13	en
dc.identifier.volume	2002	en
dc.identifier.spage	105	en
dc.identifier.epage	110	en