Australian Journal of Chemistry

Nitrones and Oxaziridines. XLV. Formation of Pyrrolo [1, 2-a] indoles by Intramolecular Nitrone Cycloaddition

DS Black, DC Craig, RB Debdas, N Kumar

Index: Black, David St. C.; Craig, Donald C.; Deb-Das, Renu B.; Kumar, Naresh Australian Journal of Chemistry, 1993 , vol. 46, # 5 p. 603 - 622

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Citation Number: 9

Abstract

Abstract The N-allylindole-2-carbaldehydes (5)-(8) and related methyl ketones (9)-(12) undergo reaction with N-methylhydroxylamine to give the cycloadducts (14)-(17) and (19)- (22), respectively. These adducts contain isoxazolidine rings fused to pyrrolo [1, 2-a] indole

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