Matches in SemOpenAlex for { <https://semopenalex.org/work/W2742214997> ?p ?o ?g. }
- W2742214997 endingPage "6479" @default.
- W2742214997 startingPage "6458" @default.
- W2742214997 abstract "Since the seminal studies from the groups of MacMillan, Stephenson and Yoon, visible light (400-700 nm) photoredox catalysis has been established as a powerful strategy to facilitate activation of organic molecules and invention of novel synthetic methodologies. Indeed, recent days, this protocol enables the syntheses of diversely functionalized organic molecules such as coerulescines, pseudotabersonines, drugs, agro chemicals, etc. Generally, activation of the redox-active functional groups of the radical precursors including diazonium salts, iodoniumsalts, sulfoniumsalts, phosphate esters, amines and sulfonyl chlorides is achieved via single-electron transfer from a photocatalyst excited by visible light irradiation sources. To date, some important reviews are available that summarize the visible light photoredox catalyses of various classes of organic compounds. To the best of our knowledge, however, there is still no review article exclusively discourses about the visible light induced productions and applications of radical species of sulfonyl chlorides (AASO2Cl, AA=alkyl/aryl). Therefore, in this review, we provide an overview on the visible light assisted procedures employed for the production of radical intermediates from sulfonyl chlorides. In addition, here we account the applications of these radical species in the syntheses of bi(hetero)aryls, difluoromethyl lactones, difluoromethyl pyrrolidines, polycyclic aromatic compounds, sulfones, trifluoromethyl (hetero)aryls, α-trifluoromethyl ketones and so on." @default.
- W2742214997 created "2017-08-17" @default.
- W2742214997 creator A5031947058 @default.
- W2742214997 creator A5032670745 @default.
- W2742214997 date "2017-07-31" @default.
- W2742214997 modified "2023-09-27" @default.
- W2742214997 title "Visible Light Photoredox Activation of Sulfonyl Chlorides: Applications in Organic Synthesis" @default.
- W2742214997 cites W129845126 @default.
- W2742214997 cites W1530826051 @default.
- W2742214997 cites W1740065139 @default.
- W2742214997 cites W1845534172 @default.
- W2742214997 cites W1966047870 @default.
- W2742214997 cites W1967290844 @default.
- W2742214997 cites W1973609141 @default.
- W2742214997 cites W1975230391 @default.
- W2742214997 cites W1978489013 @default.
- W2742214997 cites W1980122702 @default.
- W2742214997 cites W1980915688 @default.
- W2742214997 cites W1981223815 @default.
- W2742214997 cites W1981237298 @default.
- W2742214997 cites W1982809324 @default.
- W2742214997 cites W1983401069 @default.
- W2742214997 cites W1985066293 @default.
- W2742214997 cites W1986799924 @default.
- W2742214997 cites W1990365098 @default.
- W2742214997 cites W1991463958 @default.
- W2742214997 cites W1994179009 @default.
- W2742214997 cites W1994546592 @default.
- W2742214997 cites W1996941025 @default.
- W2742214997 cites W1997727718 @default.
- W2742214997 cites W1999601844 @default.
- W2742214997 cites W2001086298 @default.
- W2742214997 cites W2001701443 @default.
- W2742214997 cites W2002078338 @default.
- W2742214997 cites W2004007876 @default.
- W2742214997 cites W2004174458 @default.
- W2742214997 cites W2008726180 @default.
- W2742214997 cites W2010981957 @default.
- W2742214997 cites W2012615651 @default.
- W2742214997 cites W2017602598 @default.
- W2742214997 cites W2017685895 @default.
- W2742214997 cites W2020317621 @default.
- W2742214997 cites W2020787556 @default.
- W2742214997 cites W2021188145 @default.
- W2742214997 cites W2021911433 @default.
- W2742214997 cites W2026920337 @default.
- W2742214997 cites W2028049046 @default.
- W2742214997 cites W2029253088 @default.
- W2742214997 cites W2033043158 @default.
- W2742214997 cites W2033620575 @default.
- W2742214997 cites W2033638962 @default.
- W2742214997 cites W2037762011 @default.
- W2742214997 cites W2043172521 @default.
- W2742214997 cites W2045505563 @default.
- W2742214997 cites W2047492063 @default.
- W2742214997 cites W2051822378 @default.
- W2742214997 cites W2056252763 @default.
- W2742214997 cites W2057124754 @default.
- W2742214997 cites W2058842633 @default.
- W2742214997 cites W2061721892 @default.
- W2742214997 cites W2063300297 @default.
- W2742214997 cites W2063915017 @default.
- W2742214997 cites W2064191254 @default.
- W2742214997 cites W2064598812 @default.
- W2742214997 cites W2065304985 @default.
- W2742214997 cites W207396953 @default.
- W2742214997 cites W2076254245 @default.
- W2742214997 cites W2077621718 @default.
- W2742214997 cites W2077895811 @default.
- W2742214997 cites W2079822650 @default.
- W2742214997 cites W2080402976 @default.
- W2742214997 cites W2081910612 @default.
- W2742214997 cites W2083334069 @default.
- W2742214997 cites W2085138648 @default.
- W2742214997 cites W2085712428 @default.
- W2742214997 cites W2086657586 @default.
- W2742214997 cites W2087152379 @default.
- W2742214997 cites W2089553882 @default.
- W2742214997 cites W2091374680 @default.
- W2742214997 cites W2092727584 @default.
- W2742214997 cites W2094129737 @default.
- W2742214997 cites W2097765179 @default.
- W2742214997 cites W2105276976 @default.
- W2742214997 cites W2110134194 @default.
- W2742214997 cites W2110312043 @default.
- W2742214997 cites W2116087305 @default.
- W2742214997 cites W2119913861 @default.
- W2742214997 cites W2123455069 @default.
- W2742214997 cites W2125579691 @default.
- W2742214997 cites W2136803810 @default.
- W2742214997 cites W2143036996 @default.
- W2742214997 cites W2144869962 @default.
- W2742214997 cites W2144929531 @default.
- W2742214997 cites W2151665469 @default.
- W2742214997 cites W2152322059 @default.
- W2742214997 cites W2152775636 @default.
- W2742214997 cites W2152919588 @default.
- W2742214997 cites W2153177968 @default.