Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Bismuth(III) trifluoromethanesulfonate [Bi(OTf)3] mediated mild electrophilic aromatic formylation utilizing difluoro(phenylsulfanyl)methane (PhSCF2H) as a formylating agent in hexafluoro-2-propanol (HFIP) as a recyclable ionizing solvent has b...
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th-mahidol.454852019-08-23T17:49:26Z Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane Nolan M. Betterley Sutthichat Kerdphon Suppisak Chaturonrutsamee Sopanat Kongsriprapan Panida Surawatanawong Darunee Soorukram Manat Pohmakotr Pher G. Andersson Vichai Reutrakul Chutima Kuhakarn Kasetsart University Mahidol University Arrhenius Laboratory International Laboratories Corp. Chemistry © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Bismuth(III) trifluoromethanesulfonate [Bi(OTf)3] mediated mild electrophilic aromatic formylation utilizing difluoro(phenylsulfanyl)methane (PhSCF2H) as a formylating agent in hexafluoro-2-propanol (HFIP) as a recyclable ionizing solvent has been developed. The active formylating species was generated via C−F bond cleavage and was characterized to be a bis(phenylsulfanyl)methyl cation by experimental and computational 1H and 13C NMR. 2019-08-23T10:49:26Z 2019-08-23T10:49:26Z 2018-08-01 Article Asian Journal of Organic Chemistry. Vol.7, No.8 (2018), 1642-1647 10.1002/ajoc.201800313 21935807 2-s2.0-85051440073 https://repository.li.mahidol.ac.th/handle/123456789/45485 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051440073&origin=inward |
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Chemistry Nolan M. Betterley Sutthichat Kerdphon Suppisak Chaturonrutsamee Sopanat Kongsriprapan Panida Surawatanawong Darunee Soorukram Manat Pohmakotr Pher G. Andersson Vichai Reutrakul Chutima Kuhakarn Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
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© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Bismuth(III) trifluoromethanesulfonate [Bi(OTf)3] mediated mild electrophilic aromatic formylation utilizing difluoro(phenylsulfanyl)methane (PhSCF2H) as a formylating agent in hexafluoro-2-propanol (HFIP) as a recyclable ionizing solvent has been developed. The active formylating species was generated via C−F bond cleavage and was characterized to be a bis(phenylsulfanyl)methyl cation by experimental and computational 1H and 13C NMR. |
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Kasetsart University |
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Kasetsart University Nolan M. Betterley Sutthichat Kerdphon Suppisak Chaturonrutsamee Sopanat Kongsriprapan Panida Surawatanawong Darunee Soorukram Manat Pohmakotr Pher G. Andersson Vichai Reutrakul Chutima Kuhakarn |
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Article |
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Nolan M. Betterley Sutthichat Kerdphon Suppisak Chaturonrutsamee Sopanat Kongsriprapan Panida Surawatanawong Darunee Soorukram Manat Pohmakotr Pher G. Andersson Vichai Reutrakul Chutima Kuhakarn |
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Nolan M. Betterley |
title |
Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
title_short |
Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
title_full |
Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
title_fullStr |
Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
title_full_unstemmed |
Bi(OTf)<inf>3</inf> Enabled C-F Bond Cleavage in HFIP: Electrophilic Aromatic Formylation with Difluoro(phenylsulfanyl)methane |
title_sort |
bi(otf)<inf>3</inf> enabled c-f bond cleavage in hfip: electrophilic aromatic formylation with difluoro(phenylsulfanyl)methane |
publishDate |
2019 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/45485 |
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1763489796339007488 |