1,3-Dipolar Cycloaddition Reaction of alpha-Methylene-gamma-lactones

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Authors	MAZAL Ctibor ČASTULÍK Jakub
Year of publication	2000
Type	Article in Proceedings
Conference	XXIVth Conference of Organic Chemists on Advances in Organic Chemistry. Proceedings
MU Faculty or unit	Faculty of Science
Citation
Field	Organic chemistry
Keywords	stereoselectivity; methylene lactones; 1;3-dipolar cycloaddition
Description	Diastereo- and regioselectivity of 1,3-dipolar cycloaddition reaction of aplha-methylene lactones with azomethine ylides and photochemically generated nitrile ylide were studied.
Related projects:	Structure and character of bonding, properties and analysis of synthetic and natural molecular ensembles