Enantioselective synthesis of 3,4-dihydropyran-2-ones by domino Michael addition and lactonization with new asymmetric organocatalysts: Cinchona-alkaloid-derived chiral quaternary ammonium phenoxides

Chemistry - An Asian Journal

Volumn 2, Issue 1, 2007, Pages 123-134

  Tozawa, Takashi ^a,b   Nagao, Hitoshi ^a   Yamane, Yoshinobu ^a   Mukaiyama, Teruaki ^a,c  

^a KITASATO INSTITUTE   (Japan)

^b MITSUBISHI TANABE PHARMA CORPORATION   (Japan)

^c KITASATO UNIVERSITY   (Japan)

Author keywords

Alkaloids; Dihydropyranones; Domino reactions; Michael addition; Organocatalysis

Indexed keywords

CINCHONA ALKALOID; LACTONE; OXIDE; PYRAN DERIVATIVE; QUATERNARY AMMONIUM DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CINCHONA; STEREOISOMERISM; SYNTHESIS;

CATALYSIS; CINCHONA; CINCHONA ALKALOIDS; LACTONES; MOLECULAR STRUCTURE; OXIDES; PYRANS; QUATERNARY AMMONIUM COMPOUNDS; STEREOISOMERISM;

EID: 33846367349     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200600228     Document Type: Article

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