Abstract
Nucleophilic racemic amines have been synthesized utilizing a C7nC5x free-radical cascade reaction from a bis-allyl amine starting material. Being potentially useful organocatalytic bases as is evident from their screening in the Baylis–Hillman reaction, optically pure amines were also synthesized from optically pure aldehydes (−) or (+)-4. Bis-allyl amides under similar radical reaction condition resulted in C7n cyclized products.
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