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Communication

Chem. Commun., 2006, 2388 - 2390, DOI: 10.1039/b602937j


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

Kevin B. Bahnck and Scott D. Rychnovsky


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

Graphical abstract image for this article  (ID: b602937j)