1,3-Dipolar cycloaddition of nitrones to sugar enlactones

DOI: 10.1016/S0040-4020(01)96057-0

Source and publish data:

Tetrahedron p. 10087 - 10094 (1991)

Update date:2022-08-06

Topics:

Authors:

Panfil Panfil

Belzecki

Urbanczyk-Lipkowska

Chmielewski

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Article abstract of DOI:10.1016/S0040-4020(01)96057-0

It was found that 1,3-dipolar cycloaddition of nitrones derived from formaldehyde and acetaldehyde to sugar enlactones proceeds regio- and stereospecifically to afford anti-endo adducts.

Full text of DOI:10.1016/S0040-4020(01)96057-0

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