Regio- and Stereoselective 1,3-Dipolar Cycloaddition of Arylnitrile Oxides to 5-Acetoxy-2(5H)-furanone

DOI: 10.1007/BF00809361

Source and publish data:

Monatshefte fur Chemie p. 165 - 170 (1991)

Update date:2022-09-26

Topics: Characterization Yield Isolation Stereoselective Reaction Conditions 1,3-Dipolar Cycloaddition Regioselective

Authors:

Oravec, Peter

Fisera, Lubor

Gazo, Roman

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Article abstract of DOI:10.1007/BF00809361

Arylnitrile oxides undergo regio- and stereo-specific 1,3-dipolar cycloaddition reactions with 5-acetoxy-2(5H)-furanone.In each case a single product 3a-3g results from an anti approach to the 5-acetoxy substituent, the oxygen of the 1,3-dipole being atta

Full text of DOI:10.1007/BF00809361

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