Selectfluor®-enabled photochemical selective C(sp)-H(sulfonyl)amidation

Transition metal- and photosensitizer-free C(sp 3 )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive m...

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Published inChemical communications (Cambridge, England) Vol. 59; no. 1; pp. 118 - 121
Main Authors Chen, Yuehua, Yang, Boxuan, Li, Qian-Yu, Lin, Yu-Mei, Gong, Lei
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 22.12.2022
Royal Society of Chemistry
Subjects
Catalysis
Chemistry
Chemistry, Multidisciplinary
Diazonium Compounds
Molecular Structure
Natural products
Oxidizing agents
Physical Sciences
Reagents
Science & Technology
Selectivity
Toluene
Transition metals
FUNCTIONALIZATION
AMIDATION
AMINATION
HYDROCARBONS
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Abstract Transition metal- and photosensitizer-free C(sp 3 )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N -containing products under mild conditions in good yield and with high chemo- and site-selectivity. Chemo- and site-selective C(sp 3 )-H sulfonylamidation and amidation of toluene derivatives, cycloalkanes, natural products and bioactive molecules has been achieved by employing Selectfluor® as a versatile reagent.
AbstractList Transition metal- and photosensitizer-free C(sp3)-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N-containing products under mild conditions in good yield and with high chemo- and site-selectivity.Transition metal- and photosensitizer-free C(sp3)-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N-containing products under mild conditions in good yield and with high chemo- and site-selectivity.
Transition metal- and photosensitizer-free C(sp 3 )–H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N -containing products under mild conditions in good yield and with high chemo- and site-selectivity.
Transition metal- and photosensitizer-free C(sp 3 )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N -containing products under mild conditions in good yield and with high chemo- and site-selectivity. Chemo- and site-selective C(sp 3 )-H sulfonylamidation and amidation of toluene derivatives, cycloalkanes, natural products and bioactive molecules has been achieved by employing Selectfluor® as a versatile reagent.
Transition metal- and photosensitizer-free C(sp )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into -containing products under mild conditions in good yield and with high chemo- and site-selectivity.
Transition metal- and photosensitizer-free C(sp3)–H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N-containing products under mild conditions in good yield and with high chemo- and site-selectivity.
Transition metal- and photosensitizer-free C(sp(3))-H (sulfonyl)amidation reactions have been realized by employing Selectfluor (R) as a versatile reagent, functioning as a photoactive component, a HAT precursor and an oxidant. Various toluene derivatives, cycloalkanes, natural products and bioactive molecules can be converted into N-containing products under mild conditions in good yield and with high chemo- and site-selectivity.
Author Lin, Yu-Mei
Gong, Lei
Yang, Boxuan
Chen, Yuehua
Li, Qian-Yu
AuthorAffiliation Xiamen University
College of Chemistry and Chemical Engineering
Key Laboratory of Chemical Biology of Fujian Province
Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM)
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Cites_doi 10.1021/acscatal.9b01394
10.1021/acs.orglett.0c00081
10.1021/acs.orglett.9b00744
10.1126/science.287.5460.1995
10.1038/s41929-019-0357-9
10.1021/ar200318q
10.1002/anie.201201666
10.1039/D2CC03283J
10.1039/C7GC03149A
10.1002/anie.202013478
10.1021/jacs.8b09251
10.1039/b110638d
10.1038/446391a
10.31635/ccschem.021.202101465
10.1021/acs.orglett.5b03069
10.1002/asia.202000011
10.1016/j.tet.2011.04.054
10.1016/j.tetlet.2012.03.137
10.1016/j.tet.2019.05.043
10.1021/acs.oprd.9b00424
10.1038/s41467-019-08413-9
10.1021/acs.chemrev.6b00644
10.1002/anie.201801280
10.1126/science.abb4688
10.1002/anie.201809930
10.1039/D1GC00175B
10.1126/science.aap7503
10.1021/acscatal.9b00623
10.1002/cjoc.202200435
10.1016/S1872-2067(21)63953-0
10.1002/ange.201201945
10.1039/C7QO00547D
10.1039/c2ob26857d
10.1039/C9QO00638A
10.1038/s41557-018-0020-0
10.1021/acs.joc.8b00982
10.1038/s41467-021-22690-3
10.1039/c9qo00638a
10.1039/d2cc03283j
10.1055/s-0036-1588693
10.1055/s-0037-1610380
10.1039/c7gc03149a
10.1039/c7qo00547d
10.1039/d1gc00175b
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References Nasrallah (D2CC05569D/cit2c/1) 2020; 24
Li (D2CC05569D/cit20a/1) 2019; 2
Roizen (D2CC05569D/cit3c/1) 2012; 45
Zhang (D2CC05569D/cit20d/1) 2022; 43
Zhang (D2CC05569D/cit1/1) 2019
Sakaguchi (D2CC05569D/cit6c/1) 2002
Liang (D2CC05569D/cit17/1) 2019; 21
Chen (D2CC05569D/cit5/1) 2000; 287
Park (D2CC05569D/cit7a/1) 2017; 117
Laudadio (D2CC05569D/cit6d/1) 2020; 369
Danahy (D2CC05569D/cit14/1) 2018; 57
Yamaguchi (D2CC05569D/cit3a/1) 2012; 51
Dequirez (D2CC05569D/cit3d/1) 2012; 124
Wu (D2CC05569D/cit8c/1) 2020; 22
Narobe (D2CC05569D/cit12/1) 2022; 58
González-Esguevillas (D2CC05569D/cit13/1) 2019; 75
Lu (D2CC05569D/cit8b/1) 2018; 20
Clarke (D2CC05569D/cit2a/1) 2018; 10
Hou (D2CC05569D/cit22/1) 2021; 60
Yang (D2CC05569D/cit11/1) 2020; 15
Hazelard (D2CC05569D/cit3b/1) 2017; 4
Chen (D2CC05569D/cit10/1) 2017
Zhang (D2CC05569D/cit8a/1) 2012; 10
Akulov (D2CC05569D/cit18/1) 2021; 23
Wu (D2CC05569D/cit6b/1) 2016; 18
Niu (D2CC05569D/cit16/1) 2019; 10
Hua (D2CC05569D/cit15/1) 2019; 9
Cao (D2CC05569D/cit20c/1) 2021; 12
Wang (D2CC05569D/cit23/1) 2019; 6
Bergman (D2CC05569D/cit6a/1) 2007; 446
Li (D2CC05569D/cit20b/1) 2018; 140
Hong (D2CC05569D/cit3e/1) 2018; 359
Ramesh (D2CC05569D/cit7b/1) 2012; 53
Cao (D2CC05569D/cit20e/1) 2022; 4
Zhao (D2CC05569D/cit2b/1) 2019; 58
Yamaguchi (D2CC05569D/cit4/1) 2012; 51
Nasrallah (D2CC05569D/cit7c/1) 2020; 24
Cheng (D2CC05569D/cit19/1) 2022; 40
Bume (D2CC05569D/cit9/1) 2018; 83
Ye (D2CC05569D/cit7d/1) 2021; 67
Yang (D2CC05569D/cit21/1) 2019; 9
Yamaguchi, J (WOS:000308043900007) 2012; 51
Laudadio, G (WOS:000548751700052) 2020; 369
Cao, S (WOS:000871903100002) 2022; 4
Bergman, RG (WOS:000245079500030) 2007; 446
Hong, SY (WOS:000426366200038) 2018; 359
Ye, YH (WOS:000291778000024) 2011; 67
Nasrallah, A (WOS:000535293600011) 2020; 24
Hua, AM (WOS:000464075700060) 2019; 9
Li, YJ (WOS:000451496800043) 2018; 140
Park, Y (WOS:000405642800019) 2017; 117
Lu, XB (WOS:000419060600006) 2018; 20
Zhang, SN (WOS:000752454100004) 2022; 43
Sakaguchi, S (WOS:000174220200059) 2002
Zhao, XH (WOS:000455818400045) 2019; 58
Clark, JR (WOS:000432991800004) 2018; 10
Cao, S (WOS:000642744500008) 2021; 12
Danahy, KE (WOS:000432382800058) 2018; 57
Liang, XA (WOS:000464247500108) 2019; 21
Dequirez, G. (000893523300001.8) 2012; 124
González-Esguevillas, M (WOS:000479025900004) 2019; 75
Hou, ZW (WOS:000596791400001) 2021; 60
Zhang, Y (WOS:000310809800004) 2012; 10
Chen, K (WOS:000402749400008) 2017; 28
Wu, SW (WOS:000367702400001) 2016; 18
Chen, HY (WOS:000085902800054) 2000; 287
Wang, LH (WOS:000484262900014) 2019; 6
Akulov, AA (WOS:000628913600017) 2021; 23
Cheng, SY (WOS:000855039300001) 2022; 40
Roizen, JL (WOS:000305321100013) 2012; 45
Narobe, R (WOS:000826185800001) 2022; 58
Bume, DD (WOS:000442451500001) 2018; 83
Niu, LB (WOS:000456829100003) 2019; 10
Yang, K (WOS:000517334200001) 2020; 15
Hazelard, D (WOS:000416065700032) 2017; 4
Zhang, H (WOS:000453240600007) 2019; 51
Li, YJ (WOS:000496965000013) 2019; 2
Ramesh, D (WOS:000304387800027) 2012; 53
Wu, F (WOS:000526331100005) 2020; 22
Yang, HB (WOS:000471212600102) 2019; 9
References_xml – volume: 9
  start-page: 5708
  year: 2019
  ident: D2CC05569D/cit21/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b01394
– volume: 22
  start-page: 2135
  year: 2020
  ident: D2CC05569D/cit8c/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.0c00081
– volume: 21
  start-page: 2441
  year: 2019
  ident: D2CC05569D/cit17/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b00744
– volume: 287
  start-page: 1995
  year: 2000
  ident: D2CC05569D/cit5/1
  publication-title: Science
  doi: 10.1126/science.287.5460.1995
– volume: 2
  start-page: 1016
  year: 2019
  ident: D2CC05569D/cit20a/1
  publication-title: Nat. Catal.
  doi: 10.1038/s41929-019-0357-9
– volume: 45
  start-page: 911
  year: 2012
  ident: D2CC05569D/cit3c/1
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar200318q
– volume: 51
  start-page: 8960
  year: 2012
  ident: D2CC05569D/cit4/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201201666
– volume: 58
  start-page: 8778
  year: 2022
  ident: D2CC05569D/cit12/1
  publication-title: Chem. Commun.
  doi: 10.1039/D2CC03283J
– volume: 20
  start-page: 113
  year: 2018
  ident: D2CC05569D/cit8b/1
  publication-title: Green Chem.
  doi: 10.1039/C7GC03149A
– volume: 60
  start-page: 2943
  year: 2021
  ident: D2CC05569D/cit22/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202013478
– volume: 140
  start-page: 15850
  year: 2018
  ident: D2CC05569D/cit20b/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b09251
– start-page: 516
  year: 2002
  ident: D2CC05569D/cit6c/1
  publication-title: Chem. Commun.
  doi: 10.1039/b110638d
– volume: 446
  start-page: 391
  year: 2007
  ident: D2CC05569D/cit6a/1
  publication-title: Nature
  doi: 10.1038/446391a
– volume: 4
  start-page: 3122
  year: 2022
  ident: D2CC05569D/cit20e/1
  publication-title: CCS Chem.
  doi: 10.31635/ccschem.021.202101465
– volume: 51
  start-page: 8960
  year: 2012
  ident: D2CC05569D/cit3a/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201201666
– volume: 18
  start-page: 1
  year: 2016
  ident: D2CC05569D/cit6b/1
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b03069
– volume: 15
  start-page: 729
  year: 2020
  ident: D2CC05569D/cit11/1
  publication-title: Chem. – Asian J.
  doi: 10.1002/asia.202000011
– volume: 67
  start-page: 4649
  year: 2021
  ident: D2CC05569D/cit7d/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2011.04.054
– volume: 53
  start-page: 2904
  year: 2012
  ident: D2CC05569D/cit7b/1
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2012.03.137
– volume: 75
  start-page: 4222
  year: 2019
  ident: D2CC05569D/cit13/1
  publication-title: Tetrahedron
  doi: 10.1016/j.tet.2019.05.043
– volume: 24
  start-page: 724
  year: 2020
  ident: D2CC05569D/cit2c/1
  publication-title: Org. Process Res. Dev.
  doi: 10.1021/acs.oprd.9b00424
– volume: 10
  start-page: 467
  year: 2019
  ident: D2CC05569D/cit16/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-019-08413-9
– start-page: 640
  year: 2017
  ident: D2CC05569D/cit10/1
  publication-title: Synlett
– volume: 117
  start-page: 9247
  year: 2017
  ident: D2CC05569D/cit7a/1
  publication-title: Chem. Rev.
  doi: 10.1021/acs.chemrev.6b00644
– volume: 57
  start-page: 5134
  year: 2018
  ident: D2CC05569D/cit14/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201801280
– volume: 369
  start-page: 92
  year: 2020
  ident: D2CC05569D/cit6d/1
  publication-title: Science
  doi: 10.1126/science.abb4688
– volume: 58
  start-page: 292
  year: 2019
  ident: D2CC05569D/cit2b/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201809930
– volume: 23
  start-page: 2049
  year: 2021
  ident: D2CC05569D/cit18/1
  publication-title: Green Chem.
  doi: 10.1039/D1GC00175B
– volume: 359
  start-page: 1016
  year: 2018
  ident: D2CC05569D/cit3e/1
  publication-title: Science
  doi: 10.1126/science.aap7503
– volume: 9
  start-page: 3322
  year: 2019
  ident: D2CC05569D/cit15/1
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b00623
– volume: 40
  start-page: 2825
  year: 2022
  ident: D2CC05569D/cit19/1
  publication-title: Chin. J. Chem.
  doi: 10.1002/cjoc.202200435
– volume: 43
  start-page: 564
  year: 2022
  ident: D2CC05569D/cit20d/1
  publication-title: Chin. J. Catal.
  doi: 10.1016/S1872-2067(21)63953-0
– volume: 124
  start-page: 7498
  year: 2012
  ident: D2CC05569D/cit3d/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/ange.201201945
– start-page: 83
  year: 2019
  ident: D2CC05569D/cit1/1
  publication-title: Synthesis
– volume: 4
  start-page: 2500
  year: 2017
  ident: D2CC05569D/cit3b/1
  publication-title: Org. Chem. Front.
  doi: 10.1039/C7QO00547D
– volume: 10
  start-page: 9137
  year: 2012
  ident: D2CC05569D/cit8a/1
  publication-title: Org. Biomol. Chem.
  doi: 10.1039/c2ob26857d
– volume: 6
  start-page: 2934
  year: 2019
  ident: D2CC05569D/cit23/1
  publication-title: Org. Chem. Front.
  doi: 10.1039/C9QO00638A
– volume: 10
  start-page: 583
  year: 2018
  ident: D2CC05569D/cit2a/1
  publication-title: Nat. Chem.
  doi: 10.1038/s41557-018-0020-0
– volume: 83
  start-page: 8803
  year: 2018
  ident: D2CC05569D/cit9/1
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.8b00982
– volume: 24
  start-page: 724
  year: 2020
  ident: D2CC05569D/cit7c/1
  publication-title: Org. Process Res. Dev.
  doi: 10.1021/acs.oprd.9b00424
– volume: 12
  start-page: 2377
  year: 2021
  ident: D2CC05569D/cit20c/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-021-22690-3
– volume: 9
  start-page: 5708
  year: 2019
  ident: WOS:000471212600102
  article-title: Catalyst-Controlled C-H Functionalization of Adamantanes Using Selective H-Atom Transfer
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b01394
– volume: 10
  start-page: ARTN 467
  year: 2019
  ident: WOS:000456829100003
  article-title: Visible light-induced direct α C-H functionalization of alcohols
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/s41467-019-08413-9
– volume: 124
  start-page: 7498
  year: 2012
  ident: 000893523300001.8
  publication-title: Angew. Chem.
– volume: 6
  start-page: 2934
  year: 2019
  ident: WOS:000484262900014
  article-title: Copper-catalyzed 1,3-aminoazidation of arylcyclopropanes: a facile access to 1,3-diamine derivatives
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo00638a
– volume: 369
  start-page: 92
  year: 2020
  ident: WOS:000548751700052
  article-title: C(sp3)-H functionalizations of light hydrocarbons using decatungstate photocatalysis in flow
  publication-title: SCIENCE
  doi: 10.1126/science.abb4688
– volume: 67
  start-page: 4649
  year: 2011
  ident: WOS:000291778000024
  article-title: Cobalt-catalyzed benzylic C-H amination via dehydrogenative-coupling reaction
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2011.04.054
– volume: 57
  start-page: 5134
  year: 2018
  ident: WOS:000432382800058
  article-title: Benzylic Fluorination of Aza-Heterocycles Induced by Single-Electron Transfer to Selectfluor
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201801280
– volume: 287
  start-page: 1995
  year: 2000
  ident: WOS:000085902800054
  article-title: Thermal, catalytic, regiospecific functionalization of alkanes
  publication-title: SCIENCE
– volume: 58
  start-page: 292
  year: 2019
  ident: WOS:000455818400045
  article-title: Asymmetric Stepwise Reductive Amination of Sulfonamides, Sulfamates, and a Phosphinamide by Nickel Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201809930
– volume: 58
  start-page: 8778
  year: 2022
  ident: WOS:000826185800001
  article-title: C(sp3)-H Ritter amination by excitation of in situ generated iodine(iii)-BF3 complexes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/d2cc03283j
– volume: 40
  start-page: 2825
  year: 2022
  ident: WOS:000855039300001
  article-title: Recent Advances in Asymmetric Transformations of Unactivated Alkanes and Cycloalkanes through Direct C-H Functionalization
  publication-title: CHINESE JOURNAL OF CHEMISTRY
  doi: 10.1002/cjoc.202200435
– volume: 22
  start-page: 2135
  year: 2020
  ident: WOS:000526331100005
  article-title: Halogen-Bond-Induced Consecutive Csp3-H Aminations via Hydrogen Atom Transfer Relay Strategy
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.0c00081
– volume: 45
  start-page: 911
  year: 2012
  ident: WOS:000305321100013
  article-title: Metal-Catalyzed Nitrogen-Atom Transfer Methods for the Oxidation of Aliphatic C-H Bonds
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar200318q
– volume: 60
  start-page: 2943
  year: 2021
  ident: WOS:000596791400001
  article-title: Site-Selective Electrochemical Benzylic C-H Amination
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.202013478
– volume: 28
  start-page: 640
  year: 2017
  ident: WOS:000402749400008
  article-title: NHC-AuCl/Selectfluor: An Efficient Catalytic System for π-Bond Activation
  publication-title: SYNLETT
  doi: 10.1055/s-0036-1588693
– volume: 140
  start-page: 15850
  year: 2018
  ident: WOS:000451496800043
  article-title: Copper(II)-Catalyzed Asymmetric Photoredox Reactions: Enantioselective Alkylation of Imines Driven by Visible Light
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b09251
– volume: 51
  start-page: 83
  year: 2019
  ident: WOS:000453240600007
  article-title: Electrochemical/Photochemical Aminations Based on Oxidative Cross-Coupling between C-H and N-H
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0037-1610380
– volume: 117
  start-page: 9247
  year: 2017
  ident: WOS:000405642800019
  article-title: Transition Metal-Catalyzed C-H Amination: Scope, Mechanism, and Applications
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/acs.chemrev.6b00644
– volume: 24
  start-page: 724
  year: 2020
  ident: WOS:000535293600011
  article-title: Catalytic Intermolecular C(sp3)-H Amination with Sulfamates for the Asymmetric Synthesis of Amines
  publication-title: ORGANIC PROCESS RESEARCH & DEVELOPMENT
  doi: 10.1021/acs.oprd.9b00424
– volume: 21
  start-page: 2441
  year: 2019
  ident: WOS:000464247500108
  article-title: Visible-Light-Induced C(sp3)-H Oxidative Arylation with Heteroarenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b00744
– volume: 18
  start-page: 1
  year: 2016
  ident: WOS:000367702400001
  article-title: Metal-Free Microwave-Assisted Decarboxylative Elimination for the Synthesis of Olefins
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b03069
– volume: 83
  start-page: 8803
  year: 2018
  ident: WOS:000442451500001
  article-title: Catalyzed and Promoted Aliphatic Fluorination
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.8b00982
– volume: 15
  start-page: 729
  year: 2020
  ident: WOS:000517334200001
  article-title: Recent Advances in the Application of Selectfluor as a "Fluorine-free" Functional Reagent in Organic Synthesis
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.202000011
– start-page: 516
  year: 2002
  ident: WOS:000174220200059
  article-title: First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst
  publication-title: CHEMICAL COMMUNICATIONS
– volume: 51
  start-page: 8960
  year: 2012
  ident: WOS:000308043900007
  article-title: C-H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201201666
– volume: 20
  start-page: 113
  year: 2018
  ident: WOS:000419060600006
  article-title: Rhodium-catalyzed intermolecular C(sp3)-H amination in a purely aqueous system
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c7gc03149a
– volume: 53
  start-page: 2904
  year: 2012
  ident: WOS:000304387800027
  article-title: DDQ-mediated direct oxidative coupling of amides with benzylic and allylic sp3 C-H bonds under metal-free conditions
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2012.03.137
– volume: 359
  start-page: 1016
  year: 2018
  ident: WOS:000426366200038
  article-title: Selective formation of γ-lactams via C-H amidation enabled by tailored iridium catalysts
  publication-title: SCIENCE
  doi: 10.1126/science.aap7503
– volume: 4
  start-page: 2500
  year: 2017
  ident: WOS:000416065700032
  article-title: Catalytic C-H amination at its limits: challenges and solutions
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c7qo00547d
– volume: 10
  start-page: 583
  year: 2018
  ident: WOS:000432991800004
  article-title: Manganese-catalysed benzylic C(sp3)-H amination for late-stage functionalization
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/s41557-018-0020-0
– volume: 10
  start-page: 9137
  year: 2012
  ident: WOS:000310809800004
  article-title: Au(III)-catalyzed intermolecular amidation of benzylic C-H bonds
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c2ob26857d
– volume: 9
  start-page: 3322
  year: 2019
  ident: WOS:000464075700060
  article-title: Experimental and Theoretical Evidence for Nitrogen-Fluorine Halogen Bonding in Silver-Initiated Radical Fluorinations
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b00623
– volume: 12
  start-page: ARTN 2377
  year: 2021
  ident: WOS:000642744500008
  article-title: Photocatalytic three-component asymmetric sulfonylation via direct C(sp3)-H functionalization
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/s41467-021-22690-3
– volume: 2
  start-page: 1016
  year: 2019
  ident: WOS:000496965000013
  article-title: Photocatalytic regio- and stereoselective C(sp3)-H functionalization of benzylic and allylic hydrocarbons as well as unactivated alkanes
  publication-title: NATURE CATALYSIS
  doi: 10.1038/s41929-019-0357-9
– volume: 23
  start-page: 2049
  year: 2021
  ident: WOS:000628913600017
  article-title: Blue-light-promoted radical C-H azolation of cyclic nitrones enabled by Selectfluor®
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d1gc00175b
– volume: 75
  start-page: 4222
  year: 2019
  ident: WOS:000479025900004
  article-title: Photoredox-catalyzed deoxyfluorination of activated alcohols with Selectfluor®
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2019.05.043
– volume: 43
  start-page: 564
  year: 2022
  ident: WOS:000752454100004
  article-title: Photocatalyzed site-selective C(sp3)-H sulfonylation of toluene derivatives and cycloalkanes with inorganic sulfinates
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(21)63953-0
– volume: 446
  start-page: 391
  year: 2007
  ident: WOS:000245079500030
  article-title: Organometallic chemistry - C-H activation
  publication-title: NATURE
  doi: 10.1038/446391a
– volume: 4
  start-page: 3122
  year: 2022
  ident: WOS:000871903100002
  article-title: Nickel-Catalyzed Regiodivergent Asymmetric Cycloadditions of ?,?-Unsaturated Carbonyl Compounds
  publication-title: CCS CHEMISTRY
  doi: 10.31635/ccschem.021.202101465
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Snippet Transition metal- and photosensitizer-free C(sp 3 )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent,...
Transition metal- and photosensitizer-free C(sp 3 )–H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent,...
Transition metal- and photosensitizer-free C(sp(3))-H (sulfonyl)amidation reactions have been realized by employing Selectfluor (R) as a versatile reagent,...
Transition metal- and photosensitizer-free C(sp )-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent,...
Transition metal- and photosensitizer-free C(sp3)–H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent,...
Transition metal- and photosensitizer-free C(sp3)-H (sulfonyl)amidation reactions have been realized by employing Selectfluor® as a versatile reagent,...
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SubjectTerms Catalysis
Chemistry
Chemistry, Multidisciplinary
Diazonium Compounds
Molecular Structure
Natural products
Oxidizing agents
Physical Sciences
Reagents
Science & Technology
Selectivity
Toluene
Transition metals
Title Selectfluor®-enabled photochemical selective C(sp)-H(sulfonyl)amidation
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