Journal
SYNLETT
Volume 26, Issue 3, Pages 307-312Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1379500
Keywords
nickel; catalyst; cycloaddition; 2aminopyridnes; regiose lectivity
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Funding
- NIH [GM076125]
- NSF [0911017]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0911017] Funding Source: National Science Foundation
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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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