ChemInform Abstract: A Facile Synthesis of 3H-Indolium Perchlorates by One-Pot Hydrazone...

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2001 indole derivatives, isoindole derivatives indole derivatives, isoindole derivatives R 0140 23 - 098 A Facile Synthesis of 3H-Indolium Perchlorates by One-Pot Hy- drazone Formation/Fischer Indolization. Twenty-eight indolium salts like (III) and (VI) are prepared by reaction of phenylhydrazines (I) and (IV), α-branched ketones (II) and (V), and perchloric acid via in situ formed hydrazones. This one-pot synthesis is of high practical significance because it works without high pressure or sonochemical activation. Moreover, the products precipitate as crystals and hence the compounds are well separable solids which contain practically no impurities. The scope and limitations of this facile method are discussed. — (ZIMMERMANN, THOMAS; J. Heterocycl. Chem. 37 (2000) 6, 1571-1574; Inst. Org. Chem., Univ. Leipzig, D-04103 Leipzig, Germany; EN) 1

Transcript of ChemInform Abstract: A Facile Synthesis of 3H-Indolium Perchlorates by One-Pot Hydrazone...

Page 1: ChemInform Abstract: A Facile Synthesis of 3H-Indolium Perchlorates by One-Pot Hydrazone Formation/Fischer Indolization.

2001 indole derivatives, isoindole derivatives

indole derivatives, isoindole derivativesR 0140

23 - 098A Facile Synthesis of 3H-Indolium Perchlorates by One-Pot Hy-drazone Formation/Fischer Indolization. — Twenty-eight indoliumsalts like (III) and (VI) are prepared by reaction of phenylhydrazines (I) and(IV), α-branched ketones (II) and (V), and perchloric acid via in situ formedhydrazones. This one-pot synthesis is of high practical significance because itworks without high pressure or sonochemical activation. Moreover, the productsprecipitate as crystals and hence the compounds are well separable solids whichcontain practically no impurities. The scope and limitations of this facilemethod are discussed. — (ZIMMERMANN, THOMAS; J. Heterocycl. Chem.37 (2000) 6, 1571-1574; Inst. Org. Chem., Univ. Leipzig, D-04103 Leipzig,Germany; EN)

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