Total synthesis of marine alkaloids (ยฑ)-
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Hideaki Muratake; Mitsutaka Natsume
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Article
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1989
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Elsevier Science
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French
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Marine alkaloids hapalindoles J 1 and M 2 were concisely synthesized in the racemic form from a tertiary alcohol 4 by way of 7, 9, 11, and 17, using unusual LiAlH4 reduction of fl as a key reaction step. Hapalindoles and related indole derivatives are antibacterial and antimycotic alkaloids obtained