Email this article The Grandberg reaction in the synthesis of biologically active compounds
- Authors: Przheval’skii N.M.1, Laipanov R.K.1, Tokmakov G.P.1, Nam N.L.1
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Affiliations:
- Russian State Agrarian University–Moscow Timiryazev Agricultural Academy
- Issue: Vol 65, No 7 (2016)
- Pages: 1709-1715
- Section: Reviews
- URL: https://bakhtiniada.ru/1066-5285/article/view/238515
- DOI: https://doi.org/10.1007/s11172-016-1499-4
- ID: 238515
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Abstract
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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About the authors
N. M. Przheval’skii
Russian State Agrarian University–Moscow Timiryazev Agricultural Academy
Author for correspondence.
Email: prjevalski@mail.ru
Russian Federation, 49 ul. Timiryazevskaya, Moscow, 119991
R. K. Laipanov
Russian State Agrarian University–Moscow Timiryazev Agricultural Academy
Email: prjevalski@mail.ru
Russian Federation, 49 ul. Timiryazevskaya, Moscow, 119991
G. P. Tokmakov
Russian State Agrarian University–Moscow Timiryazev Agricultural Academy
Email: prjevalski@mail.ru
Russian Federation, 49 ul. Timiryazevskaya, Moscow, 119991
N. L. Nam
Russian State Agrarian University–Moscow Timiryazev Agricultural Academy
Email: prjevalski@mail.ru
Russian Federation, 49 ul. Timiryazevskaya, Moscow, 119991
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