期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 69, 期 4, 页码 1364-1367出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo030234b
关键词
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The anion of 2-aryl acetonitrile derivatives reacted with a variety of heteroaryl chlorides or bromides in an SNAr manifold to afford intermediate anions which were susceptible to oxidation. The addition of sodium peroxide and aqueous NH4OAc solution effected oxidation to afford aryl heteroaryl ketones in good yields. Aryl acetonitrile derivatives are thus umpolung-type synthons of the corresponding aryl carbonyl functionality.
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