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Palladium-Catalyzed C鈥揅 Triple Bond Cleavage: Efficient Synthesis of 4H-Benzo[d][1,3]oxazin-4-ones
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  • 作者:Qilun Liu ; Pinhong Chen ; Guosheng Liu
  • 刊名:ACS Catalysis
  • 出版年:2013
  • 出版时间:February 1, 2013
  • 年:2013
  • 卷:3
  • 期:2
  • 页码:178-181
  • 全文大小:316K
  • 年卷期:v.3,no.2(February 1, 2013)
  • ISSN:2155-5435
文摘
Described herein is a new transformation of azidoalkynes by using a palladium catalyst, which involves a tandem process of aminopalladation of the alkyne and oxidative rearrangement. The reaction affords a variety of 4H-benzo[d][1,3]oxazin-4-ones. Mechanism studies support a Pd-catalyzed aminopalladation/oxidation/Baeyer鈥揤illiger fragmentary sequence.

Keywords:

Pd catalyst; azidoalkyne; aminocyclization; C鈭扖 triple bond cleavage; oxidation

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