Issue 1, 2004

Participation of substituents at the ortho position of aryl groups in the rearrangements of 5-chloro-3-aryl-2,1-benzisoxazoles

Abstract

The substituent at the ortho position of the aryl groups of 5-chloro-3-aryl-2,1-benzisoxazoles is responsible for the ability of these structures to undergo rearrangements into acridinones under various conditions.

Article information

Article type
Communication
Submitted
14 Aug 2003

Mendeleev Commun., 2004,14, 37-38

Participation of substituents at the ortho position of aryl groups in the rearrangements of 5-chloro-3-aryl-2,1-benzisoxazoles

V. Yu. Orlov, A. D. Kotov, V. V. Ganzha and V. G. Sokolov, Mendeleev Commun., 2004, 14, 37 DOI: 10.1070/MC2004v014n01ABEH001846

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