4.7 Article

2,3-disubstituted indoles through the palladium-catalyzed reaction of aryl chlorides with o-alkynyltrifluoroacetanilides

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 348, Issue 10-11, Pages 1301-1305

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200606060

Keywords

alkynes; aminopalladation-reductive elimination; cyclization; indoles; palladium

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2,3-Disubstituted indoles can be prepared in moderate to excellent yields by reacting readily available o-alkynyltrifluoroacetanilides with aryl chlorides in MeCN at 120 degrees C in the presence of Pd-2(dba)(3) and Xphos.

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