Stereochemical studies on the 1,3-dipolar cycloaddition of 3,4,5,6-tetrahydropyridine 1-oxide to 2(5H)-furanones

Pau Cid, Pedro de March, Marta Figueredo, Josep Font, Sergio Milán

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Resum

The 1,3-dipolar cycloaddition of 3,4,5,6-tetrahydropyridine 1-oxide, 1, to 2(5H)-furanones 2, 3, and 4 is investigated. Crucial nmr data are indicated to determine the conformational equilibria and stereochemistry of the adducts. The major products arise from exo transition states. © 1992.
Idioma originalAnglès
Pàgines (de-a)667-670
RevistaTetrahedron Letters
Volum33
Número5
DOIs
Estat de la publicacióPublicada - 28 de gen. 1992

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