Stereocontrolled synthesis of 1,3,5-triols by tandem hydroboration/carbonyl reduction

DOI: 10.1016/0040-4039(92)89037-D

Source and publish data:

Tetrahedron Letters p. 5807 - 5810 (1992)

Update date:2022-08-02

Topics:

Authors:

Harada, Toshiro

Imanaka, Satoru

Ohyama, Yoshimitsu

Matsuda, Yasuhiro

Oku, Akira

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Article abstract of DOI:10.1016/0040-4039(92)89037-D

A highly convergent method for the stereoselective synthesis of 1,3,5-triol frameworks has been developed by utilizing a tandem hydroboration/carbonyl reduction of β-silyl-γ,δ-unsaturated ketones 2 with thexylborane.

Full text of DOI:10.1016/0040-4039(92)89037-D

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