ACYLAMINOACETYL DERIVATIVES OF ACTIVE METHYLENE-COMPOUNDS .3. C-ACYLATION REACTIONS VIA THE HIPPURIC-ACID AZLACTONE

HAMILAKIS, S; KONTONASSIOS, D; SANDRIS, C

dc.contributor.author	HAMILAKIS, S	en
dc.contributor.author	KONTONASSIOS, D	en
dc.contributor.author	SANDRIS, C	en
dc.date.accessioned	2014-03-01T01:42:44Z
dc.date.available	2014-03-01T01:42:44Z
dc.date.issued	1994	en
dc.identifier.issn	0022-152X	en
dc.identifier.uri	https://dspace.lib.ntua.gr/xmlui/handle/123456789/23923
dc.subject.classification	Chemistry, Organic	en
dc.subject.other	SUBSTITUTED TETRAMIC ACIDS	en
dc.subject.other	CYCLIZATION	en
dc.subject.other	ANHYDRIDES	en
dc.title	ACYLAMINOACETYL DERIVATIVES OF ACTIVE METHYLENE-COMPOUNDS .3. C-ACYLATION REACTIONS VIA THE HIPPURIC-ACID AZLACTONE	en
heal.type	journalArticle	en
heal.language	English	en
heal.publicationDate	1994	en
heal.abstract	The C-acylation reactions of the active methylene compounds, methyl cyanoacetate and Meldrum's acid, with hippuric acid, using the DCC activation and the mixed anhydride conditions, are shown to proceed through initial formation of 2-phenyl-5(4H)-oxazolone, the hippuric acid azlactone. The conditions of these reactions using the azlactone as the acylating agent were investigated and discussed.	en
heal.publisher	HETERO CORPORATION	en
heal.journalName	JOURNAL OF HETEROCYCLIC CHEMISTRY	en
dc.identifier.isi	ISI:A1994PL21900008	en
dc.identifier.volume	31	en
dc.identifier.issue	5	en
dc.identifier.spage	1145	en
dc.identifier.epage	1150	en