Regio- and Stereoselective 1,3-Dipolar Cycloaddition of Arylnitrile Oxides to 5-Acetoxy-2(5H)-furanone
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
Oravec, Peter,Fisera, Lubor,Gazo, Roman
p. 165 - 170
(2007/10/02)
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