Issue 7, 1982

Enantioselective 1,5-electrocyclization. Synthesis of optically active indolines

Abstract

Intramolecular base-catalysed 1,5-elecctrocyclization of aldehyde imines derived from o-aminophenyl succinimide (3) in the presence of a chiral alcohol yields chiral indolines (4) with optical purities ranging from 17 to 31%.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 369-370

Enantioselective 1,5-electrocyclization. Synthesis of optically active indolines

S. J. Veenstra and W. N. Speckamp, J. Chem. Soc., Chem. Commun., 1982, 369 DOI: 10.1039/C39820000369

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