Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis

Literature Information

Publication Date 2006-05-02
DOI 10.1039/B602937J
Impact Factor 6.222
Authors

Kevin B. Bahnck, Scott D. Rychnovsky


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Abstract

Prins cyclization using an electron-rich benzaldehyde and a homoallylic alcohol efficiently delivered the fully substituted C-aryl tetrahydropyranoside of kendomycin.

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Contents list

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Front cover

Cover

DOI: 10.1039/C7EW90023F

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