期刊
ORGANIC LETTERS
卷 12, 期 10, 页码 2306-2309出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol100666v
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-
资金
- National Institutes of Health [GM 48498]
A versatile method for the synthesis of 3,3-diaryloxindoies via Pd-catalyzed alpha-arylations or an SNAr reaction is described. The reaction proceeds using mild base, is tolerant of a variety of functional groups, and is capable of preparing hindered all-carbon quaternary centers.
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