Mechanism of stereoselective synthesis of push-pull (Z)-4-oxothiazolidine derivatives containing an exocyclic double bond. A MNDO-PM3 Study

dc.creator	Marković, R.
dc.creator	Vitnik, Ž.
dc.creator	Baranac-Stojanović, Marija
dc.creator	Juranić, Ivan O.
dc.date.accessioned	2018-11-22T00:04:17Z
dc.date.available	2018-11-22T00:04:17Z
dc.date.issued	2002
dc.identifier.issn	0308-2342
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/52
dc.description.abstract	Calculations using the MNDO-PM3 method were performed to elucidate the mechanism of stereoselective base-catalyzed reaction affording exclusively (Z)-2-alkylidene-4-oxothiazolidine push-pull derivatives from the corresponding α-mercapto esters and activated β-oxonitriles in ethanol as a solvent.	en
dc.rights	restrictedAccess
dc.source	Journal of Chemical Research. Synopses
dc.subject	MNDO-PM3	en
dc.subject	Z-2-alkylidene-4-oxothiazolidine	en
dc.title	Mechanism of stereoselective synthesis of push-pull (Z)-4-oxothiazolidine derivatives containing an exocyclic double bond. A MNDO-PM3 Study	en
dc.type	article
dc.rights.license	ARR
dc.citation.issue	10
dc.citation.spage	485
dc.citation.epage	489
dc.citation.other	(10): 485-489
dc.citation.rank	M23
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-0036816392
dc.identifier.rcub	https://hdl.handle.net/21.15107/rcub_cherry_52