The Grandberg reaction in the synthesis of biologically active compounds


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The review is focused on the Grandberg synthesis, namely, the synthesis of tryptamines from arylhydrazines and γ-halocarbonyl compounds, as an exceptionally useful and efficient methodology to access biologically active indole heterocycles.

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N. Przheval’skii

Russian State Agrarian University–Moscow Timiryazev Agricultural Academy

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Email: prjevalski@mail.ru
俄罗斯联邦, 49 ul. Timiryazevskaya, Moscow, 119991

R. Laipanov

Russian State Agrarian University–Moscow Timiryazev Agricultural Academy

Email: prjevalski@mail.ru
俄罗斯联邦, 49 ul. Timiryazevskaya, Moscow, 119991

G. Tokmakov

Russian State Agrarian University–Moscow Timiryazev Agricultural Academy

Email: prjevalski@mail.ru
俄罗斯联邦, 49 ul. Timiryazevskaya, Moscow, 119991

N. Nam

Russian State Agrarian University–Moscow Timiryazev Agricultural Academy

Email: prjevalski@mail.ru
俄罗斯联邦, 49 ul. Timiryazevskaya, Moscow, 119991

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