New synthetic route to granulatimide and its structural analogues

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Abstract

The Stille coupling reaction of stannylindole 12 with 4-iodoimidazole 13 (or 24) in the presence of PdCl2(PPh3)2 gave the corresponding indole-imidazole coupling product 14 (or 25), thereby affording a new synthetic approach to the alkaloid granulatimide (7), isolated from the Brazilian ascidian Didemnum granulatum, as well as its structural analogues, 10-methylgranulatimide (23), 17-methylgranulatimide (30), 10,17-dimethylgranulatimide (31). © 2002 Pharmaceutical Society of Japan.

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Yoshida, T., Nishiyachi, M., Nakashima, N., Murase, M., & Kotani, E. (2002). New synthetic route to granulatimide and its structural analogues. Chemical and Pharmaceutical Bulletin, 50(6), 872–876. https://doi.org/10.1248/cpb.50.872

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