The Addition of Diallylzinc to 5-Substituted 4,5-Dihydroisoxazoles

Abstract
The addition of diallyl zinc to a range of 5-aryl-4,5-dihydroisoxazoles, occurs with a diastereoselectivity of between 6.9 : 1 and 3.6 : 1. The major product is the trans isomer as demonstrated by an X-ray crystal structure on the phenyl thiourea derivative of one of the major products.

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