Chiral Bifunctional Thiourea-Catalyzed Enantioselective Michael Addition of Ketones to Nitrodienes
Hai Ma, Kun Liu, Fa‐Guang Zhang, Chuanle Zhu, Jing Nie, Jun‐An Ma
Abstract
Hai Ma, Kun Liu, Fa‐Guang Zhang, Chuanle Zhu, Jing Nie, Jun‐An Ma
Abstract
Simple bifunctional thioureas, derived from the commercially available saccharides and chiral diamines, have been shown tunably to promote Michael-type addition of ketones to alpha,beta-gamma,delta-nitrodienes. The Michael adducts were obtained in good yields albeit with high enantioselectivites (84-99% ee). Furthermore, these products can be readily transformed into more useful molecules.
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Simple bifunctional thioureas, derived from the commercially available saccharides and chiral diamines, have been shown tunably to promote Michael-type addition of ketones to alpha,beta-gamma,delta-nitrodienes. The Michael adducts were obtained in good yields albeit with high enantioselectivites (84-99% ee). Furthermore, these products can be readily transformed into more useful molecules.
Key concepts: Bifunctional, Chemistry, Michael reaction, Thiourea, Enantioselective synthesis, Adduct, Organic chemistry, Catalysis