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July 18, 2001Organic Letters272 citations

Gold(III) Chloride Catalyzed Cyclization of α-Hydroxyallenes to 2,5-Dihydrofurans

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AHAnja Hoffmann‐RöderNKNorbert Krause

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Abstract

reaction: see text Functionalized alpha-hydroxyallenes 1 were smoothly converted into the corresponding 2,5-dihydrofurans 2 by using 5-10 mol % of gold(III) chloride as catalyst. This mild and efficient cyclization method can be applied to alkyl- and alkenyl-substituted allenes at room temperature, furnishing tri- and tetrasubstituted dihydrofurans in good to excellent chemical yields and with complete axis to center chirality transfer.

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Hoffmann‐Röder et al. (2001) studied this question.

synapsesocial.com/papers/6a0e28c47a57fdc4e227b2fdhttps://doi.org/10.1021/ol016205+
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