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ChemInform Abstract: An Enantioselective Synthesis of Natural (-)-Huperzine A via Cinchona Alkaloid Promoted Asymmetric Michael Reaction.

✍ Scribed by S. KANEKO; T. YOSHINO; T. KATOH; S. TERASHIMA


Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis


An Enantioselective Synthesis of Natural (-)-Huperzine A via Cinchona Alkaloid Promoted Asymmetric Michael Reaction.

-An improved synthesis of the title compound is developed via the known intermediate (+)-(III) derived from the Ξ²-keto ester (I). After one recrystallization (+)-(III) is obtainable with 99% e.e. The synthesis of the enantiomer (-)-(III) is also possible by this method using (+)-cinchonine.

-(KANEKO, S.;


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