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Fischer indole synthesis

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Fischer indole synthesis

[‚fish·ər ′in‚dōl ‚sin·thə·səs]
(organic chemistry)
A reaction to form indole derivatives by means of a ring closure of aromatic hydrazones.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
References in periodicals archive
Sarojini, Synthesis of Some New Biologically Active 1,3,4-oxadiazolyl nitroindoles and a Modified Fischer Indole Synthesis of Ethyl Nitro Indole-2-carboxylates.
A Facile Route towards the Synthesis of 2-(1H-indol-3-yl)-acetamides Using 1,1-Carbonyldiimidazole
Fischer indole synthesis (3) (sometimes called Fischer indolization) is one of the oldest and most convenient, and it is currently used for a broad range of applications.
Fischer indole synthesis of 2-methoxyphenylhydrazone (5)
(1982) In The Fischer Indole Synthesis. John Wiley and Sons, New York, p.
(1997) A novel method for suppression of the abnormal Fischer indole synthesis. Tetrahedron 53, 8853-8870.
(1999) Thermal cyclization of N-trifluoroacetyl enehydrazines under milder conditions: A novel entry into the Fischer indole synthesis. Tetrahedron Lett.
Peculiarity of methoxy group-substituted phenylhydrazones in Fischer indole synthesis
Peculiarity of methoxy group- substituted phenylhydrazones in Fischer indole synthesis Yasuoki MURAKAMI Communicated by Takao SEKIYA, M.J.A.
Proceedings at the 1054th General Meeting
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