Selective formation of new solvent-derived products from ozonolyses of 1-acetoxy- and 1-chloro-2,3-diphenylindene

Kevin J. McCullough, Tomohiro Fujisaka, Masatomo Nojima, Shigekazu Kusabayashi

Research output: Contribution to journalArticlepeer-review

Abstract

Ozonlysis of solutions of 1-acetoxy- and 1-chloro-2,3-diphenylindene in methanol at -70° C afford, via a highly selective rearrangement of the corresponding intermediate primary ozonides, a seven-membered cyclic hemiperacetal and an isochroman derivative respectively whose structures have been determined unambiguously by X-ray analysis. © 1988.

Original languageEnglish
Pages (from-to)3375-3378
Number of pages4
JournalTetrahedron Letters
Volume29
Issue number27
Publication statusPublished - 1988

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