One-step Synthesis for the Preparation of Quinoline Alkaloid Analogues

Zografos, AL; Mitsos, CA; Igglessi-Markopoulou, O

dc.contributor.author	Zografos, AL	en
dc.contributor.author	Mitsos, CA	en
dc.contributor.author	Igglessi-Markopoulou, O	en
dc.date.accessioned	2014-03-01T01:14:58Z
dc.date.available	2014-03-01T01:14:58Z
dc.date.issued	1999	en
dc.identifier.issn	1523-7060	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/13281
dc.subject.classification	Chemistry, Organic	en
dc.subject.other	SILYL ENOL ETHERS	en
dc.subject.other	TITANIUM TETRACHLORIDE	en
dc.title	One-step Synthesis for the Preparation of Quinoline Alkaloid Analogues	en
heal.type	journalArticle	en
heal.identifier.primary	10.1021/ol9911021	en
heal.identifier.secondary	http://dx.doi.org/10.1021/ol9911021	en
heal.language	English	en
heal.publicationDate	1999	en
heal.abstract	(Matrix Presented) A new one-step methodology has been introduced for the synthesis of quinoline alkaloid analogues. The reaction is based on a modification of the Mukaiyama aldol condensation, making use of the high reactivity of lactones or anhrydrides. The reaction is general and allows for the construction of new hetero polycondenced molecules in a one-step synthesis.	en
heal.publisher	AMER CHEMICAL SOC	en
heal.journalName	Organic Letters	en
dc.identifier.doi	10.1021/ol9911021	en
dc.identifier.isi	ISI:000084980300021	en
dc.identifier.volume	1	en
dc.identifier.issue	12	en
dc.identifier.spage	1953	en
dc.identifier.epage	1955	en