کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1315190 | 1499368 | 2009 | 10 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Nucleophilic, radical, and electrophilic (phenylsulfonyl)difluoromethylations Nucleophilic, radical, and electrophilic (phenylsulfonyl)difluoromethylations](/preview/png/1315190.png)
Selective incorporation of a fluoroalkyl moiety to modulate the properties of an organic molecule has become a frequently used strategy in life science- and materials science-related applications. In this context, selective introduction of a (phenylsulfonyl)difluoromethyl group (PhSO2CF2) into organic molecules has attracted much attention, since the PhSO2CF2 group can be regarded as a “chemical chameleon” that can be readily transformed into difluoromethyl (CF2H), difluoromethylene (–CF2–), and difluoromethylidene (CF2) functionalities. This article overviews the recent development of (phenylsulfonyl)difluoromethylation reactions from 2003, including the nucleophilic (phenylsulfonyl)difluoromethylations with PhSO2CF2H, PhSO2CF2SiMe3 and PhSO2CF2Br reagents, free radical (phenylsulfonyl)difluoromethylations with PhSO2CF2I reagent, and electrophilic (phenylsulfonyl)difluoromethylations with a hypervalent iodine(III)-CF2SO2Ph reagent.
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Journal: Journal of Fluorine Chemistry - Volume 130, Issue 12, December 2009, Pages 1130–1139