4.4 Article

3,5-Disubstituted 2-Aminopyridines via Nickel-Catalyzed Cyclo-addition of Terminal Alkynes and Cyanamides

期刊

SYNLETT
卷 26, 期 3, 页码 307-312

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1379500

关键词

nickel; catalyst; cycloaddition; 2aminopyridnes; regiose lectivity

资金

  1. NIH [GM076125]
  2. NSF [0911017]
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [0911017] Funding Source: National Science Foundation

向作者/读者索取更多资源

The regioselectivity of the Ni/SIPr-catalyzed cyc addition terminal alkynes and cyanamides was explored. In general, 3,5-disubstituted 2-aminopyridines were formed as the major product.

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