Palladium-catalyzed esterification of aryl halides using aryl formates without the use of external carbon monoxide.
نویسندگان
چکیده
Aryl formates are efficient carbon monoxide sources in palladium-catalyzed esterification of aryl halides. The carbonylation readily proceeds at ambient pressure without the use of external carbon monoxide to afford the corresponding esters in high yields.
منابع مشابه
Carbon monoxide free aminocarbonylation of aryl and alkenyl iodides using DMF as an amide source.
[reaction: see text] Palladium-catalyzed coupling reaction of N,N-dimethylformamide with aryl or alkenyl halides successfully proceeded in the presence of phosphoryl chloride to afford the corresponding tertiary amides in good yields.
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We describe here a tandem catalytic route to prepare imidazoles in a single operation from aryl iodides, imines and CO. The reaction involves a catalytic carbonylation of aryl halides with imines to form 1,3dipoles, which undergo spontaneous 1,3-dipolar cycloaddition. Overall, this offers an alternative to coupling reactions to construct the (hetero)aryl-imidazole motif, where variation of the ...
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ورودعنوان ژورنال:
- Chemical communications
دوره 48 64 شماره
صفحات -
تاریخ انتشار 2012