3-Arylpyrrolidines via azomethine ylide 1,3-dipolar cycloaddition to styrenes
Monosubstituted olefins conjugated to an aromatic or heteroaromatic ring undergo 1,3-dipolar cycloaddition with the azomethie ylide derived from N-benzyl-N-(methoxymethyl)trimethylsilylamine to give 3-aryl- and 3-hetero-arylpyrrolidines in good to excellent yield.
Laborde, Edgardo
p. 6607 - 6610
(2007/10/02)
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