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2000
Volume 3, Issue 3
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

α-Diazo-β-ketophosphonates, bearing an oxygen atom adjacent to the γ position, led mainly or exclusively to compounds derived from a Wolff rearrangement when submitted to the action of a catalytic amount of Rh(II) in refluxing toluene. It is suggested that the presence of this inductive withdrawing electronic atom prevents competing intramolecular C-H insertion reactions to occur.

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/content/journals/loc/10.2174/157017806775789877
2006-03-01
2025-09-10
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/content/journals/loc/10.2174/157017806775789877
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  • Article Type:
    Research Article
Keyword(s): Ketenes; Rhodiocarbenoid; Wolff rearrangement; α-Diazo-β-keto-compounds
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