Enantioselective Synthesis of Cordiachro
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Samir Bouzbouz; Jean-Yves Goujon; JerΓ΄me Deplanne; Bernard Kirschleger
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Article
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2000
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John Wiley and Sons
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English
β 317 KB
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An enantioselective synthesis of cordiachromene is described. An allylic alcohol moiety is first attached in the oposition to the methoxymethoxy substituent in 1-methoxy-4methoxymethoxybenzene. Then chirality is introduced successively through asymmetric Sharpless epoxidation on the allylic alcohol