Download - ChemInform Abstract: Stereoselectivity of Triplet Photocycloadditions. Part 10. Oxazole—Carbonyl Photocycloadditions: Selectivity Pattern and Synthetic Route to erythro α-Amino,

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2000 oxazole derivatives

oxazole derivativesR 0220

31 - 132Stereoselectivity of Triplet Photocycloadditions. Part 10. Oxazole–Carbonyl Photocycloadditions: Selectivity Pattern and SyntheticRoute to erythro α-Amino, β-Hydroxy Ketones. — The photocycload-dition of aliphatic and aromatic aldehydes (IIa)–(IIc) with oxazole (I) proceedshighly regio- and stereoselectively to give bicyclic oxetanes (III). Hydrolyticcleavage of these adducts gives selectively erythro α-amino, β-hydroxy methylketones. — (GRIESBECK, AXEL G.; FIEGE, MAREN; LEX, JOHANN;Chem. Commun. (Cambridge) (2000) 7, 589-590; Inst. Org. Chem., Univ.Koeln, D-50939 Koeln, Germany; EN)

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