Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227146 | Tetrahedron | 2009 | 10 Pages |
Abstract
Site-selective direct arylation of both sp2 and sp3 sites on azine N-oxide substrates is described. The arylation reactions are carried out in either a divergent manner or a sequential manner. The sp3 arylation reaction is applied to the synthesis of the natural products, papaverine and crykonisine, and a rationale for low reactivity of electron-deficient aryl halides is provided. Mechanistic investigations point toward the intimate involvement of the base in the mechanism of these reactions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Derek J. Schipper, Louis-Charles Campeau, Keith Fagnou,