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Use of allylic boranes in organic syntheses. Synthesis of an analog of the alkaloid flustrabromine

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Abstract

The analog of the alkaloid flustrabromine containing no Br atom in position 6 was obtained in three steps. The key step involves reductive prenylation of 3-R-indole with triprenylborane.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

    I. V. Zhun & A. V. Ignatenko

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  1. I. V. Zhun
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  2. A. V. Ignatenko
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2126–2128, October, 2004.

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Zhun, I.V., Ignatenko, A.V. Use of allylic boranes in organic syntheses. Synthesis of an analog of the alkaloid flustrabromine. Russ Chem Bull 53, 2221–2223 (2004). https://doi.org/10.1007/s11172-005-0103-0

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  • DOI: https://doi.org/10.1007/s11172-005-0103-0

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