3-Cyano-3-methoxycarbonyl-2,4,4,5-tetraphenylpyrrolidine as a precursor of benzylidenammonium benzylide

Abstract
On being heated in refluxing toluene, 3-cyano-3-methoxycarbonyl-2,4,4,5-tetraphenylpyrrolidine undergoes a retro-1,3-dipolar cycloaddition to yield benzylidenammonium benzylide, which is trapped by some dipolarophiles.

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