Enantioselective Conjugate Addition of Alkynes to Thioamides
N. Kumagai, Masakatsu Shibasaki, Ryo Yazaki
Abstract
N. Kumagai, Masakatsu Shibasaki, Ryo Yazaki
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.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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