Enantioselective Access to Key Intermediates for Salvinorin A and Analogues
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説明
<jats:title>Abstract</jats:title><jats:p>Access to enantiopure synthetic platforms that can generate key intermediates for salvinorin A analogues through diastereoselective Diels–Alder cycloaddition between an enantiopure sulfinylquinone and semicyclic dienes is described.</jats:p>
収録刊行物
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- European Journal of Organic Chemistry
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European Journal of Organic Chemistry 2011 (15), 2818-2826, 2011-04-07
Wiley