Radical Cyclization Routes to Bridged Pyranosides as Precursors of Densely Functionalized Cycloalkanes

DOI: 10.1021/jo00028a033

Source and publish data:

Journal of Organic Chemistry p. 573 - 584 (1992)

Update date:2022-09-26

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Authors:

Alonso, R. A.

Vite, G. D.

McDevitt, R. E.

Fraser-Reid, B.

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Article abstract of DOI:10.1021/jo00028a033

Glycals derived from hexapyranoses permit the incorporation of iodine at C-2 as well as elaboration of an olefinic residue via the C-5-hydroxymethyl group.Radical cyclization of these functionalities leads to bicyclic systems whose bridge sizes depend on

Full text of DOI:10.1021/jo00028a033

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