Ruthenium Catalysed N-Heterocyclisation: Indoles from 2-Aminophenethyl Alcohols

DOI: 10.1039/c39860001575

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1575 - 1576 (1986)

Update date:2022-08-28

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Authors:

Tsuji, Yasushi

Huh, Keun-Tae

Yokoyama, Yasuharu

Watanabe, Yoshihisa

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Article abstract of DOI:10.1039/c39860001575

Dichlorotris(triphenylphosphine)ruthenium is highly active as a catalyst for the N-heterocyclisation of 2-aminophenethyl alcohols (2a-d) into indole derivatives in toluene under reflux, and the reactions proceed with spontaneous hydrogen evolution.

Full text of DOI:10.1039/c39860001575

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