Akai_2005_Chem.Commun.(Camb)__2369

Reference

Title : Lipase-catalyzed domino kinetic resolution of alpha-hydroxynitrones\/intramolecular 1,3-dipolar cycloaddition: a concise asymmetric total synthesis of (-)-rosmarinecine - Akai_2005_Chem.Commun.(Camb)__2369
Author(s) : Akai S , Tanimoto K , Kanao Y , Omura S , Kita Y
Ref : Chem Commun (Camb) , :2369 , 2005
Abstract :

The title domino reactions were developed to directly provide tetrahydrofuro[3,4-c]isoxazole derivatives (5 and 9) in > or =90% ee from racemic alpha-hydroxynitrones (2 and 6), which were used in the concise asymmetric total synthesis of (-)-rosmarinecine .

PubMedSearch : Akai_2005_Chem.Commun.(Camb)__2369
PubMedID: 15877131

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Citations formats

Akai S, Tanimoto K, Kanao Y, Omura S, Kita Y (2005)
Lipase-catalyzed domino kinetic resolution of alpha-hydroxynitrones\/intramolecular 1,3-dipolar cycloaddition: a concise asymmetric total synthesis of (-)-rosmarinecine
Chem Commun (Camb) :2369

Akai S, Tanimoto K, Kanao Y, Omura S, Kita Y (2005)
Chem Commun (Camb) :2369