Lewis Acid Mediated Reactions of 2,3-Epoxyalcohols: an Efficient Stereocontrolled Route to Polycyclic Diols

DOI: 10.1016/S0040-4020(01)80561-5

Source and publish data:

Tetrahedron p. 10339 - 10354 (1993)

Update date:2022-08-29

Topics:

Authors:

Marson, Charles M.

Harper, Steven

Walker, Andrew J.

Pickering, Jane

Campbell, Jonathan

et al. et al.

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Article abstract of DOI:10.1016/S0040-4020(01)80561-5

2,3-epoxyalcohols are shown to undergo stereoselective reactions in the presence of tin tetrachloride.The resulting diols when treated with acid are converted into polycyclic aromatic hydrocarbons or polycyclic ketones.

Full text of DOI:10.1016/S0040-4020(01)80561-5

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