The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mi...The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mild reaction conditions,stoichiometric acceptor/donorless conditions(visible light photoredox catalysis)and chiral catalysts contributed to a rapid development of this intriguing research area capable of creating chemical diversity/complexity from readily available unsaturated hydrocarbons and CO2 as a C1-buinding block.The most recent developments in the field have been collected in the present review article and organized,based on the different sets ofπ-systems/intermediates/reactive partners employed(i.e.,nickelalactones,organo-halides)as well as synthetic strategies(i.e.,visible-light photo redox catalysis).展开更多
The chemodivergent ring-opening of cyclobutanols is described under the carbocatalytic assistance of graphene oxide(GO).The protocol enables the synthesis of diversely functionalized dienes or indenes(26 examples)base...The chemodivergent ring-opening of cyclobutanols is described under the carbocatalytic assistance of graphene oxide(GO).The protocol enables the synthesis of diversely functionalized dienes or indenes(26 examples)based on the amount of GO employed.Spectroscopic(XPS and ssNMR)as well as experimental investigations revealed a direct involvement of theπ-domains of GO in tuning the stability of carbocationic intermediates during the reaction.展开更多
基金Financial support by the National Key Research and Development Program of China(Grants 2017YFA0204503 and 2017YFA0207800)the National Natural Science Foundation of China(Grants 51903187,21734006 and 21975178)the China Postdoctoral Science Foundation(No.2020M670642)is gratefully acknowledged.
文摘The tandem catalytic functionalization/carboxylation of double as well as triple carbon-carbon bonds with CO_(2) represent an emerging research area in synthetic organic methodology.In particular,the combination of mild reaction conditions,stoichiometric acceptor/donorless conditions(visible light photoredox catalysis)and chiral catalysts contributed to a rapid development of this intriguing research area capable of creating chemical diversity/complexity from readily available unsaturated hydrocarbons and CO2 as a C1-buinding block.The most recent developments in the field have been collected in the present review article and organized,based on the different sets ofπ-systems/intermediates/reactive partners employed(i.e.,nickelalactones,organo-halides)as well as synthetic strategies(i.e.,visible-light photo redox catalysis).
基金financial support and to the Italian Ministry of Education,University and Research(MIUR)PRIN-2017 project 2017W8KNZWThe research leading to these results has received funding from the European Union's Horizon 2020 research and innovation programme under Graphene Core3881603-Graphene+1 种基金Flagship.F.B.and E.R.acknowledge the MIUR,and European Social Fund(ESF)for the PON R&l 2014-2020 program,action IV.4"Doctorates and research contracts on Innovation topics"This work benefited from access(ITAO17)to CERM/CIRMMP,Italy centre of Instruct-ERIC,a Landmak ESFRI project,for the ssNMR measurements and support.
文摘The chemodivergent ring-opening of cyclobutanols is described under the carbocatalytic assistance of graphene oxide(GO).The protocol enables the synthesis of diversely functionalized dienes or indenes(26 examples)based on the amount of GO employed.Spectroscopic(XPS and ssNMR)as well as experimental investigations revealed a direct involvement of theπ-domains of GO in tuning the stability of carbocationic intermediates during the reaction.
