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For: Lee C, Cook AJ, Elisabeth JE, Friede NC, Sammis GM, Ball ND. The Emerging Applications of Sulfur(VI) Fluorides in Catalysis. ACS Catal 2021;11:6578-89. [PMID: 34123485 DOI: 10.1021/acscatal.1c01201] [Cited by in Crossref: 35] [Cited by in F6Publishing: 37] [Article Influence: 35.0] [Reference Citation Analysis]
Number Citing Articles
1 Ghosh J, Mendoza J, Cooks RG. Accelerated and Concerted Aza‐Michael Addition and SuFEx Reaction in Microdroplets in Unitary and High‐Throughput Formats. Angew Chem Int Ed 2022. [DOI: 10.1002/anie.202214090] [Reference Citation Analysis]
2 Zhang H, Yang N, Li J, Wang P, Li S, Xie L, Liao S. Radical Fluorosulfonyl Arylation of Alkenes: Accessing FSO2-Functionalized Chromanes via Formal Endo and Exo Cyclization. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03224] [Reference Citation Analysis]
3 Zeng YZ, Wang JB, Qin HL. A reductive dehalogenative process for chemo- and stereoselective synthesis of 1,3-dienylsulfonyl fluorides. Org Biomol Chem 2022. [PMID: 36168842 DOI: 10.1039/d2ob01434c] [Reference Citation Analysis]
4 Wang P, Zhang H, Zhao M, Ji S, Lin L, Yang N, Nie X, Song J, Liao S. Radical Hydro‐Fluorosulfonylation of Unactivated Alkenes and Alkynes. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202207684] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Cheng Y, Li G, Smedley CJ, Giel MC, Kitamura S, Woehl JL, Bianco G, Forli S, Homer JA, Cappiello JR, Wolan DW, Moses JE, Sharpless KB. Diversity oriented clicking delivers β-substituted alkenyl sulfonyl fluorides as covalent human neutrophil elastase inhibitors. Proc Natl Acad Sci U S A 2022;119:e2208540119. [PMID: 36070343 DOI: 10.1073/pnas.2208540119] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Wang P, Li S, Zhang H, Yang N, Liao S. Photo-organocatalytic Synthesis of β-Keto Sulfonyl Fluorides via Radical Fluorosulfonylation of Vinyl Acetates. Synlett. [DOI: 10.1055/s-0041-1738692] [Reference Citation Analysis]
7 Vogel JA, Hammami R, Ko A, Datta H, Eiben YN, Labenne KJ, McCarver EC, Yilmaz EZ, Melvin PR. Synthesis of Highly Reactive Sulfone Iminium Fluorides and Their Use in Deoxyfluorination and Sulfur Fluoride Exchange Chemistry. Org Lett 2022. [PMID: 35930030 DOI: 10.1021/acs.orglett.2c02232] [Reference Citation Analysis]
8 Zhang W, Deng X, Zhang FX, Lin JH, Xiao JC, Liang SH. Synthesis and 18F Labeling of Alkenyl Sulfonyl Fluorides via an Unconventional Elimination Pathway. Org Lett 2022. [PMID: 35771975 DOI: 10.1021/acs.orglett.2c02091] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Han B, Khasnavis SR, Nwerem M, Bertagna M, Ball ND, Ogba OM. Calcium Bistriflimide-Mediated Sulfur(VI)-Fluoride Exchange (SuFEx): Mechanistic Insights toward Instigating Catalysis. Inorg Chem 2022;61:9746-55. [PMID: 35700314 DOI: 10.1021/acs.inorgchem.2c01230] [Reference Citation Analysis]
10 Wang P, Zhang H, Nie X, Xu T, Liao S. Photoredox catalytic radical fluorosulfonylation of olefins enabled by a bench-stable redox-active fluorosulfonyl radical precursor. Nat Commun 2022;13:3370. [PMID: 35690603 DOI: 10.1038/s41467-022-31089-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
11 Magre M, Ni S, Cornella J. (Hetero)aryl-SVI Fluorides: Synthetic Development and Opportunities. Angew Chem Int Ed Engl 2022;61:e202200904. [PMID: 35303387 DOI: 10.1002/anie.202200904] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 11.0] [Reference Citation Analysis]
12 Zeng D, Ma Y, Deng W, Wang M, Jiang X. Divergent sulfur(VI) fluoride exchange linkage of sulfonimidoyl fluorides and alkynes. Nat Synth 2022;1:455-463. [DOI: 10.1038/s44160-022-00060-1] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Feng Q, Fu Y, Zheng Y, Liao S, Huang S. Electrochemical Synthesis of β-Keto Sulfonyl Fluorides via Radical Fluorosulfonylation of Vinyl Triflates. Org Lett 2022. [PMID: 35579434 DOI: 10.1021/acs.orglett.2c01336] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
14 Du P, Sun Q, Li H, Zhang J, Deng H, Jiang H. Silver-catalyzed Radical Cascade Arylthiodifluoromethylation/ Cyclization of Isonitriles for the Synthesis of 6-Phenanthridinyldifluoromethyl Aryl Thioethers. Chem Asian J 2022;:e202200088. [PMID: 35319154 DOI: 10.1002/asia.202200088] [Reference Citation Analysis]
15 Yamanushkin P, Kaya K, Feliciano MAM, Gold B. SuFExable NH-Pyrazoles via 1,3-Dipolar Cycloadditions of Diazo Compounds with Bromoethenylsulfonyl Fluoride. J Org Chem 2022. [PMID: 35143195 DOI: 10.1021/acs.joc.1c03105] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
16 Ma Z, Shan L, Ma X, Hu X, Guo Y, Chen Q, Liu C. Arenesulfonyl fluoride synthesis via one-pot copper-free Sandmeyer-type three-component reaction of aryl amine, K2S2O5, and NFSI. Journal of Fluorine Chemistry 2022;254:109948. [DOI: 10.1016/j.jfluchem.2022.109948] [Reference Citation Analysis]
17 Rojas JJ, Croft RA, Sterling AJ, Briggs EL, Antermite D, Schmitt DC, Blagojevic L, Haycock P, White AJP, Duarte F, Choi C, Mousseau JJ, Bull JA. Amino-oxetanes as amide isosteres by an alternative defluorosulfonylative coupling of sulfonyl fluorides. Nat Chem 2022. [PMID: 35087220 DOI: 10.1038/s41557-021-00856-2] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
18 Smedley CJ, Homer JA, Gialelis TL, Barrow AS, Koelln RA, Moses JE. Accelerated SuFEx Click Chemistry For Modular Synthesis**. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202112375] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Lou TS, Willis MC. Sulfonyl fluorides as targets and substrates in the development of new synthetic methods. Nat Rev Chem. [DOI: 10.1038/s41570-021-00352-8] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 18.0] [Reference Citation Analysis]
20 Zhang H, Li S, Zheng H, Zhu G, Liao S, Nie X. Photocatalytic fluorosulfonylation of aliphatic carboxylic acid NHPI esters. Org Chem Front . [DOI: 10.1039/d2qo00861k] [Reference Citation Analysis]
21 Ma Z, Liu Y, Ma X, Hu X, Guo Y, Chen Q, Liu C. Aliphatic sulfonyl fluoride synthesis via reductive decarboxylative fluorosulfonylation of aliphatic carboxylic acid NHPI esters. Org Chem Front 2022;9:1115-20. [DOI: 10.1039/d1qo01655e] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
22 Song X, He Y, Wang B, Peng S, Pan X, Wei M, Liu Q, Qin H, Tang H. Synthesis of aryl sulfonyl fluorides from aryl sulfonyl chlorides using sulfuryl fluoride (SO2F2) as fluoride provider. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132657] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 He F, Li Y, Wu J. Fluorosulfonyl radicals: new horizons for the synthesis of sulfonyl fluorides. Org Chem Front . [DOI: 10.1039/d2qo01211a] [Reference Citation Analysis]
24 Cui J, Ke S, Zhao J, Wu S, Luo W, Xu S, Su X, Li Y. Photocatalytic access to aromatic keto sulfonyl fluorides from vinyl fluorosulfates. Org Chem Front 2022;9:3540-5. [DOI: 10.1039/d2qo00416j] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
25 Magre M, Cornella J. Redox-Neutral Organometallic Elementary Steps at Bismuth: Catalytic Synthesis of Aryl Sulfonyl Fluorides. J Am Chem Soc 2021;143:21497-502. [PMID: 34914387 DOI: 10.1021/jacs.1c11463] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 18.0] [Reference Citation Analysis]
26 Lee C, Thomson BJ, Sammis GM. Rapid and column-free syntheses of acyl fluorides and peptides using ex situ generated thionyl fluoride. Chem Sci 2021;13:188-94. [PMID: 35059166 DOI: 10.1039/d1sc05316g] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
27 Chen D, Nie X, Feng Q, Zhang Y, Wang Y, Wang Q, Huang L, Huang S, Liao S. Electrochemical Oxo-Fluorosulfonylation of Alkynes under Air: Facile Access to β-Keto Sulfonyl Fluorides. Angew Chem Int Ed Engl 2021;60:27271-6. [PMID: 34729882 DOI: 10.1002/anie.202112118] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 17.0] [Reference Citation Analysis]
28 Chen D, Nie X, Feng Q, Zhang Y, Wang Y, Wang Q, Huang L, Huang S, Liao S. Electrochemical Oxo‐Fluorosulfonylation of Alkynes under Air: Facile Access to β‐Keto Sulfonyl Fluorides. Angew Chem 2021;133:27477-82. [DOI: 10.1002/ange.202112118] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
29 Grygorenko OO, Volochnyuk DM, Vashchenko BV. Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances. European J Organic Chem 2021;2021:6478-510. [DOI: 10.1002/ejoc.202100857] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 11.0] [Reference Citation Analysis]
30 Pan Q, Liu Y, Pang W, Wu J, Ma X, Hu X, Guo Y, Chen QY, Liu C. Copper-catalyzed three-component reaction of arylhydrazine hydrochloride, DABSO, and NFSI for the synthesis of arenesulfonyl fluorides. Org Biomol Chem 2021;19:8999-9003. [PMID: 34605502 DOI: 10.1039/d1ob01697k] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
31 Chelagha A, Louvel D, Taponard A, Berthelon R, Tlili A. Synthetic Routes to Arylsulfonyl Fluorides. Catalysts 2021;11:830. [DOI: 10.3390/catal11070830] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]