STEREOSELECTIVE SYNTHESIS OF THE (+/-)-IRELAND ALCOHOL

DOI: 10.1016/S0040-4039(00)80738-8

Source and publish data:

Tetrahedron Letters p. 5285 - 5286 (1988)

Update date:2022-07-30

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Authors:

Ikegami, Satoru

Katsuki, Tsutomu

Yamaguchi, Masaru

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Article abstract of DOI:10.1016/S0040-4039(00)80738-8

The Ireland alcohol, a key intermediate for the synthesis of tirandamycin A, was prepared in a stereoselective manner, where titanium-mediated <2,3>Wittig rearrangement and iodolactonization were used as key steps for the construction of four consecutive asymmetric centers.

Full text of DOI:10.1016/S0040-4039(00)80738-8

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