STEREOSELECTIVE SYNTHESIS OF THE FUNCTIONALIZED SYN-1,3,5,7-TETRAOL

DOI: 10.1016/S0040-4039(00)94299-0

Source and publish data:

Tetrahedron Letters p. 3873 - 3876 (1983)

Update date:2022-08-04

Topics:

Authors:

Nakata, Tadashi

Takao, Sachiko

Fukui, Mineo

Tanaka, Tadasu

Oishi, Takeshi

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Article abstract of DOI:10.1016/S0040-4039(00)94299-0

The syn-1,3,5,7-tetraol derivative 21 was synthesized with complete stereoselection based on the stereoselective reduction of a six-membered β-keto hemiacetal and a subsequent hemiacetal ring opening.

Full text of DOI:10.1016/S0040-4039(00)94299-0

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