Deprotonative cadmation of functionalized aromatics
نویسندگان
چکیده
منابع مشابه
Deprotonative cadmation of functionalized aromatics.
This communication describes the deproto-metalation of a large range of aromatics including heterocycles using a newly developed lithium-cadmium base; the reaction proceeds at room temperature with an excellent chemoselectivity and efficiency, and proved to be regioselective in most cases.
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[1,2,3]Triazolo[1,5-a]pyridine and 3-substituted derivatives were regioselectively metalated at the 7 position using either Bu3MgLi or (TMP)3CdLi, the former at -10 degrees C and the latter at room temperature. The lithium arylmagnesates (R = H, Me, Ph) proved to react with iodine (34-75%) or 3,4,5-trimethoxybenzaldehyde (32-51%). Attempts to obtain the cross-coupling products using 2-bromopyri...
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ژورنال
عنوان ژورنال: Chemical Communications
سال: 2008
ISSN: 1359-7345,1364-548X
DOI: 10.1039/b809543d