Comprehensive Summary The conversion of CF3-alkenes to gem-difluoroalkenes using reductive cross-coupling strategy has received much attention in recent years,however,the use of green and readily available reducing sa...Comprehensive Summary The conversion of CF3-alkenes to gem-difluoroalkenes using reductive cross-coupling strategy has received much attention in recent years,however,the use of green and readily available reducing salt to mediate these reactions remains to be explored.In this work,a concise construction of gem-difluoroalkenes,which requires neither a catalyst nor a metal reducing agent,was established.Rongalite,a safe and inexpensive industrial product,was employed as both a radical initiator and reductant.This procedure was compatible with both linear and cyclic diaryliodonium salts,enabling a wide variety of substrates(>70 examples).The utility of this approach was demonstrated through gram-scale synthesis and efficient late-stage functionalizations of anti-inflammatory drugs.展开更多
This review provides a comprehensive summary of progress to date in the utilization of rongalite as a versatile reagent in organic synthesis,with a focus on recent researches.The contents have been organized according...This review provides a comprehensive summary of progress to date in the utilization of rongalite as a versatile reagent in organic synthesis,with a focus on recent researches.The contents have been organized according to the functions exhibited by rongalite.Reaction mechanisms are provided,demonstrating the multifaceted roles of this compound in various transformations,including as a sulfone,C1 or masked proton source and as a single electron donor or reducing agent.展开更多
Reduced species （HSO2^-, SO2^·-） promoted one-pot synthesis of phenyl alkyl selenides has been developed. This synthetic method was achieved by reactions of diphenyl diselenide with alkyl halides at room temper...Reduced species （HSO2^-, SO2^·-） promoted one-pot synthesis of phenyl alkyl selenides has been developed. This synthetic method was achieved by reactions of diphenyl diselenide with alkyl halides at room temperature. It is noteworthy that the reactions were operated under mild reaction conditions, required short time, and got good resuits. A single electron transfer reaction mechanism was proposed for the reaction.展开更多
基金supported by the National Natural Science Foundation of China(Grants 21971080,21971079,21772051)This work was also supported by the 111 Project B17019.
文摘Comprehensive Summary The conversion of CF3-alkenes to gem-difluoroalkenes using reductive cross-coupling strategy has received much attention in recent years,however,the use of green and readily available reducing salt to mediate these reactions remains to be explored.In this work,a concise construction of gem-difluoroalkenes,which requires neither a catalyst nor a metal reducing agent,was established.Rongalite,a safe and inexpensive industrial product,was employed as both a radical initiator and reductant.This procedure was compatible with both linear and cyclic diaryliodonium salts,enabling a wide variety of substrates(>70 examples).The utility of this approach was demonstrated through gram-scale synthesis and efficient late-stage functionalizations of anti-inflammatory drugs.
基金financial support from the the National Natural Science Foundation of China(Grants 21971080,21971079,21772051)supported by 111 Project B17019.
文摘This review provides a comprehensive summary of progress to date in the utilization of rongalite as a versatile reagent in organic synthesis,with a focus on recent researches.The contents have been organized according to the functions exhibited by rongalite.Reaction mechanisms are provided,demonstrating the multifaceted roles of this compound in various transformations,including as a sulfone,C1 or masked proton source and as a single electron donor or reducing agent.
基金Project supported by the National Natural Science Foundation of China （No. 20572079）, the Natural Science Foundation of Zhejiang Province （Nos. Y205540 and Y404039） and the Wenzhou University Postgraduate Innovation Foundation （No. YCX0514）.
文摘Reduced species （HSO2^-, SO2^·-） promoted one-pot synthesis of phenyl alkyl selenides has been developed. This synthetic method was achieved by reactions of diphenyl diselenide with alkyl halides at room temperature. It is noteworthy that the reactions were operated under mild reaction conditions, required short time, and got good resuits. A single electron transfer reaction mechanism was proposed for the reaction.
