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Chemo-Enzymatic Synthesis of the HMG-CoA Reductase Inhibitor Rosuvastatin and Natural Styryllactone Cryptomoscatone E1

ASIAN JOURNAL OF ORGANIC CHEMISTRY(2017)

Cited 9|Views17
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Abstract
Racemic syn-ethyl (E)-2-(2,2-dimethyl-6-styryl-1,3-dioxan-4-yl)acetate is hydrolyzed with high enantioselectivity by Novozyme-435 in 0.05m sodium phosphate buffer at room temperature. The optically pure unreacted ethyl 2-((4R,6S)-2,2-dimethyl-6-((E)-styryl)-1,3-dioxan-4-yl)acetate and hydrolyzed (4S,6R)-acid are used in the synthesis of HMG-CoA reductase inhibitor rosuvastatin and the naturally occurring styryl lactone cryptomoscatoneE1, respectively.
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Key words
biocatalysis,kinetic resolution,rosuvastatin,styryl lactones,total synthesis
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