NEW FUNCTIONALIZATIONS OF OXANORBORNENIC SYSTEMS VIA 1,3-DIPOLAR CYCLOADDITIONS WITH C,N-DIPHENYLNITRONE

DOI: 10.1016/S0040-4020(01)86090-7

Source and publish data:

Tetrahedron p. 7199 - 7204 (1988)

Update date:2022-07-31

Topics: 1,3-Dipolar Cycloadditions Functionalizations

Authors:

Arjona, Odon

Pradilla, Roberto Fernandez de la

Perez, Rosa A.

Plumet, Joaquin

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Article abstract of DOI:10.1016/S0040-4020(01)86090-7

The regio- and stereoselectivity of the cycloaddition between C,N-diphenylnitrone and 2-endo-acetoxy-7-oxabicyclo<2.2.1>hept-5-ene-2-exo-carbonitrile has been studied.Subsequent fragmentation of the isoxazolidine ring with mCPBA followed by acidic hydroly

Full text of DOI:10.1016/S0040-4020(01)86090-7

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