ACID-CATALYZED REARRANGEMENT OF PYRAN DERIVATIVES. AN APPROACH TO THE STEREOSELECTIVE SYNTHESIS OF 1,3-DIOL DERIVATIVES

DOI: 10.1016/S0040-4039(00)99149-4

Source and publish data:

Tetrahedron Letters p. 2885 - 2888 (1989)

Update date:2022-08-04

Topics:

Authors:

DeShong, Philip

Simpson, David M.

Lin, Ming-Teh

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Article abstract of DOI:10.1016/S0040-4039(00)99149-4

Peracid oxidation and HF-catalyzed treatment of furfuryl alcohol derivatives afford lactone products arising from a highly stereoselective rearrangement process.The lactone serve as precursors of highly functionalized anti-1,3-diol derivatives.

Full text of DOI:10.1016/S0040-4039(00)99149-4

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