Ketal-lactone compounds and their stereoselective cleavage to cyclic ethers

DOI: 10.1016/S0040-4039(97)10196-4

Source and publish data:

Tetrahedron Letters p. 8207 - 8210 (1997)

Update date:2022-08-10

Topics:

Authors:

Jun, Jong-Gab

Lee, Dong Woo

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Article abstract of DOI:10.1016/S0040-4039(97)10196-4

The easy preparation of ketal-lactone compounds via Diels-Alder reaction, followed by hydrolysis and cyclization and excellent stereoselective ring opening of the ketal-lactone to 6-membered and 7- membered cyclic ethers are described.

Full text of DOI:10.1016/S0040-4039(97)10196-4

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