alexa Abstract | A facile enantioselective synthesis of (R)-massoialactone

Journal of Chemical and Pharmaceutical Research
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A novel and highly efficient synthesis of (R)-Massoialactone employing Sharpless asymmetric epoxidation of allyl alcohol has been accomplished. The synthesis also demonstrates the effective use of regioselective reductive opening of epoxy alcohols.

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Author(s): B Narasimha Reddy and R P Singh


(R)-Massoialactone, pheromone, Sharpless epoxidation, selective hydride reduction., facile enantioselective synthesis

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