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Four novel taxoid analogs were conversionally synthesized from the C19-diterpenoid alkaloid deltaline, and their cytotoxic activities were evaluated against a small panel of cancer cell lines. [ABSTRACT FROM AUTHOR]

The regioselective demethylations of two C19-diterpenoid alkaloids, 2 and 3, have been achieved with HBr-HOAc, trimethylsilyl iodide, or BBr3. It was observed that HBr-HOAc is an optimal demethylating agent for these two C19-diterpenoid alkaloids because it could provide different O-demethylation products by using different reaction temperature and reaction time. Especially, 1-O-methyl group in 2 and 3, one of the most difficult ones to be demethylated, could be removed by the treatment with HBr-HOAc at an elevated temperature and a prolonged reaction time. [ABSTRACT FROM AUTHOR]

The conversional synthesis of taxoids by the BAC sequence from the C19-diterpenoid alkaloids, 14-acetyltalatisamine (1), yunaconitine (12), and 14-acetylchasmanine (19), was designed and explored. Two aconane-type diterpenes 17 and 28, the advanced intermediates for our conversional synthesis, were synthesized. The key steps include the rupture of the C(7)-C(17) bond, the formation of imine, and the denitrogenation. [ABSTRACT FROM AUTHOR]