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Lee, Cayo, Ball, Nicholas D., Sammis, Glenn M. (2019) One-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride. Chemical Communications, 55 (98). 14753-14756 doi:10.1039/c9cc08487h

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Reference TypeJournal (article/letter/editorial)
TitleOne-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride
JournalChemical Communications
AuthorsLee, CayoAuthor
Ball, Nicholas D.Author
Sammis, Glenn M.Author
Year2019Volume55
Issue98
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/c9cc08487hSearch in ResearchGate
Generate Citation Formats
Mindat Ref. ID8166148Long-form Identifiermindat:1:5:8166148:8
GUID0
Full ReferenceLee, Cayo, Ball, Nicholas D., Sammis, Glenn M. (2019) One-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride. Chemical Communications, 55 (98). 14753-14756 doi:10.1039/c9cc08487h
Plain TextLee, Cayo, Ball, Nicholas D., Sammis, Glenn M. (2019) One-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride. Chemical Communications, 55 (98). 14753-14756 doi:10.1039/c9cc08487h
In(2019) Chemical Communications Vol. 55 (98) Royal Society of Chemistry (RSC)

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Foth, Paul J., Gu, Frances, Bolduc, Trevor G., Kanani, Sahil S., Sammis, Glenn M. (2019) New sulfuryl fluoride-derived alkylating reagents for the 1,1-dihydrofluoroalkylation of thiols. Chemical Science, 10. 10331-10335 doi:10.1039/c9sc03570b
Lee, Cayo, Thomson, Brodie J., Sammis, Glenn M. (2022) Rapid and column-free syntheses of acyl fluorides and peptides using ex situ generated thionyl fluoride. Chemical Science, 13 (1) 188-194 doi:10.1039/d1sc05316g
Epifanov, Maxim, Foth, Paul J., Gu, Frances, Barrillon, Charlotte, Kanani, Sahil S., Higman, Carolyn S., Hein, Jason E., Sammis, Glenn M. (2018) One-Pot 1,1-Dihydrofluoroalkylation of Amines Using Sulfuryl Fluoride. Journal Of The American Chemical Society, 140 (48) 16464-16468 doi:10.1021/jacs.8b11309
Thomson, Brodie J., Khasnavis, Samuel R., Grigorian, Emma C., Krishnan, Rohun, Yassa, Theodore D., Lee, Kelvin, Sammis, Glenn M., Ball, Nicholas D. (2023) Facile synthesis of sulfonyl fluorides from sulfonic acids. Chemical Communications, 59 (5) 555-558 doi:10.1039/d2cc05781f
Foth, Paul J., Malig, Thomas C., Yu, Hao, Bolduc, Trevor G., Hein, Jason E., Sammis, Glenn M. (2020) Halide-Accelerated Acyl Fluoride Formation Using Sulfuryl Fluoride. Organic Letters, 22 (16) 6682-6686 doi:10.1021/acs.orglett.0c02566
Chappell, William P., Favié, Marie, Sammis, Glenn M. (2024) Thionyl fluoride as a sulfur(iv) SuFEx hub for the efficient syntheses of sulfinamides and sulfinate esters. Chemical Communications, 60 (72). doi:10.1039/d4cc02876g
Lee, Cayo, Lai, Joey, Epifanov, Maxim, Wang, Cindy Xinyun, Sammis, Glenn M. (2021) Efficient protocol for the SO2F2-mediated deoxyfluorination of aliphatic alcohols. Journal of Fluorine Chemistry, 251. 109888pp. doi:10.1016/j.jfluchem.2021.109888
Zhang, Yiyuan, Chen, Wanting, Tan, Tingting, Gu, Yuang, Zhang, Shuning, Li, Jie, Wang, Yan, Hou, Wei, Yang, Guang, Ma, Peixiang, Xu, Hongtao (2021) Palladium-catalyzed one-pot phosphorylation of phenols mediated by sulfuryl fluoride. Chemical Communications, 57 (37) 4588-4591 doi:10.1039/d1cc00769f
Boldrini, Cosimo, Harutyunyan, Syuzanna R. (2021) Pd-catalyzed allylative dearomatisation using Grignard reagents. Chemical Communications, 57 (89) 11807-11810 doi:10.1039/d1cc05609c
Vargová, Denisa, Pérez, Juana M., Harutyunyan, Syuzanna R., Šebesta, Radovan (2019) Trapping of chiral enolates generated by Lewis acid promoted conjugate addition of Grignard reagents to unreactive Michael acceptors by various electrophiles. Chemical Communications, 55 (78). 11766-11769 doi:10.1039/c9cc05041h
Downey, Kathleen T., Mo, Jia Yi, Lai, Joey, Thomson, Brodie J., Sammis, Glenn M. (2023) Sulfur(iv) reagents for the SuFEx-based synthesis of substituted sulfamate esters. Chemical Science, 14 (7) 1775-1780 doi:10.1039/d2sc05945b
 
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