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A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds. Issue 11 (5th January 2016)
Record Type:
Journal Article
Title:
A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds. Issue 11 (5th January 2016)
Main Title:
A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds
Abstract : The first Cu-mediated, one-pot Michael addition/α-arylation method for preparing α-aryl-β-substituted cyclic ketone scaffolds has been developed. Abstract : The direct and efficient construction of α-aryl-β-substituted cyclic ketone scaffolds has been achieved using a Cu-mediated one-pot Michael addition/α-arylation strategy. The reaction features easily available materials, broad substrate scope, moderate to good yield, and an excellent diastereoselectivity.