Invention Grant
US09073887B2 Single step enantioselective process for the preparation of 3-substituted chiral phthalides 有权
用于制备3-取代的手性苯并二氮杂萘的单步对映选择性方法

Single step enantioselective process for the preparation of 3-substituted chiral phthalides
Abstract:
The present invention discloses single step, highly enantioselective catalytic oxidative cyclization process for the synthesis of 3-substituted chiral phthalides. In particular, the invention discloses asymmetric synthesis of chiral phthalides via synergetic nitrile accelerated oxidative cyclization of o-cyano substituted aryl alkenes in high yield and enantiomeric excess (ee) in short reaction time. Also, disclosed herein is “one-pot” asymmetric synthesis of biologically important natural compounds having 3-substituted chiral phthalide structural framework in the molecule.
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