Total synthesis of urdamycinone B via C-glycosidation of an unprotected sugar and Diels-Alder reaction of C-glycosyl juglone

DOI: 10.1039/CC9960000225

Source and publish data:

Chemical Communications p. 225 - 226 (1996)

Update date:2022-08-04

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Authors:

Matsuo, Goh

Miki, Yuko

Nakata, Masaya

Matsumura, Shuichi

Toshima, Kazunobu

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Article abstract of DOI:10.1039/CC9960000225

The total synthesis of C-glycosyl angucycline, urdamycinone B 1, was achieved via C-glycosidation of naphthol 6 and the unprotected D-olivose 7, and Diels-Alder reaction of the unprotected C-glycosyl juglone 9 and the diene 17 as the key steps.

Full text of DOI:10.1039/CC9960000225

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