Pregled bibliografske jedinice broj: 296458
Chiral Chromenes: Synthesis, Separation of Enantiomers and Barriers to Reversible Ring Opening
Chiral Chromenes: Synthesis, Separation of Enantiomers and Barriers to Reversible Ring Opening // The Seventh International Course and Conference on the Interface between Manthematics, Cemistry and Computer Science
Rovinj, Hrvatska, 1992. (poster, nije recenziran, sažetak, znanstveni)
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Naslov
Chiral Chromenes: Synthesis, Separation of Enantiomers and Barriers to Reversible Ring Opening
Autori
Otočan, Klaudio ; Lončar, Linda ; Mintas, Mladen ; Trötsch, Thomas ; Mannschreck, Albrecht
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
The Seventh International Course and Conference on the Interface between Manthematics, Cemistry and Computer Science
Mjesto i datum
Rovinj, Hrvatska, 22.06.1992. - 26.06.1992
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
kiralni kromeni; sinteza; odvajanje enantiomera;
(chiral chromenes; separation of enantiomers)
Sažetak
Chromenes or 2H-benzopyrans have been the subject od extensive studies largely of their photochromic behaviour which consists in a reversible photoisomerization involving a rupture of the C (sp3) – O bond. In connection with our previous studies on 2, 2'-spirobichromenes1 we have prepared chiral chromeneses (l) and (2) in order to separate their enantiomers and determine the unknown barriers to ring opening reaction. The novel compounds (l) and (2) have been synthesized by reduction of the appropriate lactone with diisobutylaluminium hydride and subsequent O-alkylation of the resulting lactols. Separations or enrichments of enantiomers were achieved by liquid chromatography on triacetylcellulose and tribenzoylcellulose. (+)-(l) and (-)-(l) being separated almost completely, while in (2) an enrichment of enantiomers was achieved by using the recycling procedure. The barriers for reversible rin opening/ ring closure reaction of (l) and (2) were determined by thermal racemization of separated enantiomers. The mechanism of interconversion of enantiomers necessarilly requires a ring opened dienone intermediate with a most probable Z-stereostructure . Also, photochemically induced interconversion of preparatively isolated enantiomers of (+)-(l), i.e , photoracemization, was successfully performed for the first time in that class of chiral chromenes.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb