Bifunctional 3,3′-Ph2-BINOL-Mg Catalyzed Direct Asymmetric Vinylogous Michael Addition of α,β-Unsaturated γ-Butyrolactam
Li Lin, Jinlong Zhang, Xiaojuan Ma, Xu Fu, Rui Wang
Abstract
Li Lin, Jinlong Zhang, Xiaojuan Ma, Xu Fu, Rui Wang
Abstract
Bifunctional 3,3'-Ph(2)-BINOL-Mg catalyzed direct asymmetric vinylogous Michael addition of α,β-unsaturated γ-butyrolactam has been developed. The catalytic activity of this protocol was slightly affected by different types of Michael acceptors, such as a variety of enones as well as α,β-unsaturated N-acylpyrroles. The Michael products were obtained with high diastereoselectivities (up to 20:1) and excellent enantioselectivities (up to 98%).
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Bifunctional 3,3'-Ph(2)-BINOL-Mg catalyzed direct asymmetric vinylogous Michael addition of α,β-unsaturated γ-butyrolactam has been developed. The catalytic activity of this protocol was slightly affected by different types of Michael acceptors, such as a variety of enones as well as α,β-unsaturated N-acylpyrroles. The Michael products were obtained with high diastereoselectivities (up to 20:1) and excellent enantioselectivities (up to 98%).
Key concepts: Bifunctional, Michael reaction, Chemistry, Catalysis, Addition reaction, Organic chemistry, Medicinal chemistry