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Enantioselective Conjugate Addition of Alkynes to Thioamides

N. Kumagai, Masakatsu Shibasaki, Ryo Yazaki

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Abstract

Significance Enantioselective conjugate additions of alkynes are exceptionally difficult. Recent progress has been made toward this goal using highly reactive Michael acceptors. The authors present the first example of enantioselective terminal alkyne conjugate addition to unsaturated thioamides, a diverse and easily derivatized Michael acceptor.

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Significance Enantioselective conjugate additions of alkynes are exceptionally difficult. Recent progress has been made toward this goal using highly reactive Michael acceptors. The authors present the first example of enantioselective terminal alkyne conjugate addition to unsaturated thioamides, a diverse and easily derivatized Michael acceptor.

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Available abstract

Significance Enantioselective conjugate additions of alkynes are exceptionally difficult. Recent progress has been made toward this goal using highly reactive Michael acceptors. The authors present the first example of enantioselective terminal alkyne conjugate addition to unsaturated thioamides, a diverse and easily derivatized Michael acceptor.

Key concepts: Enantioselective synthesis, Conjugate, Chemistry, Alkyne, Michael reaction, Combinatorial chemistry, Addition reaction, Organic chemistry

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