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From N-benzoylpyridinium imides to pyrazolo[1,5-a]pyridines: a mechanistic discussion on a stoichiometric Cu protocol.
Ling, Lin; Chen, Jingqing; Song, Jiahui; Zhang, Yuhai; Li, Xinqian; Song, Lijuan; Shi, Feng; Li, Yuxue; Wu, Chunrui.
Affiliation
  • Ling L; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Ling Ling Road, Shanghai 200032, China.
Org Biomol Chem ; 11(23): 3894-902, 2013 Jun 21.
Article in En | MEDLINE | ID: mdl-23657368
ABSTRACT
A Cu-mediated preparation of 2-substitiuted pyrazolo[1,5-a]pyridines from N-benzoylpyridinium imides and terminal alkynes is described using stoichiometric Cu(OAc)2 as both the mediator and the oxidant. Extensive DFT calculations suggest a Cu(III) intermediate via disproportionation of Cu(II).
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Pyridinium Compounds / Copper / Imides Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Pyridinium Compounds / Copper / Imides Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2013 Document type: Article Affiliation country: China