Enantioselective Total Synthesis of Ligraminol D and Ligraminol E
Baliram B. Mane, D. D. Kumbhar, Suresh B. Waghmode
Abstract
Baliram B. Mane, D. D. Kumbhar, Suresh B. Waghmode
Abstract
As a part of our ongoing research on the synthesis of bioactive constituents or molecules by using an organocatalytic approach, enantioselective total syntheses of ligraminol D and ligraminol E were achieved starting from a commercially available nonchiral aldehyde. Key steps in this synthesis were an asymmetric α-aminoxylation of an aldehyde and a Mitsunobu reaction.
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As a part of our ongoing research on the synthesis of bioactive constituents or molecules by using an organocatalytic approach, enantioselective total syntheses of ligraminol D and ligraminol E were achieved starting from a commercially available nonchiral aldehyde. Key steps in this synthesis were an asymmetric α-aminoxylation of an aldehyde and a Mitsunobu reaction.
Key concepts: Enantioselective synthesis, Aldehyde, Chemistry, Total synthesis, Mitsunobu reaction, Organic chemistry, Stereochemistry, Combinatorial chemistry