Synergistic cooperative effect of CF3SO2Na and bis(2-butoxyethyl)ether towards selective oxygenation of sulfides with molecular oxygen under visible-light irradiation

A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF3SO2Na...

Full description

Saved in:
Bibliographic Details
Published inGreen chemistry : an international journal and green chemistry resource : GC Vol. 23; no. 1; pp. 496 - 500
Main Authors Liu, Kai-Jian, Wang, Zheng, Lu, Ling-Hui, Chen, Jin-Yang, Zeng, Fei, Lin, Ying-Wu, Cao, Zhong, Yu, Xianyong, He, Wei-Min
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 07.01.2021
Royal Society of Chemistry
Subjects
Online AccessGet full text

Cover

Loading…
Abstract A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF3SO2Na and 2-butoxyethyl ether represents the key promoting factor for the reaction.
AbstractList A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF₃SO₂Na and 2-butoxyethyl ether represents the key promoting factor for the reaction.
A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at ambient temperature under transition-metal-, additives-free and minimal solvent conditions. The synergistic catalytic efforts between CF3SO2Na and 2-butoxyethyl ether represents the key promoting factor for the reaction.
Author Zeng, Fei
Yu, Xianyong
Liu, Kai-Jian
Wang, Zheng
He, Wei-Min
Lin, Ying-Wu
Chen, Jin-Yang
Cao, Zhong
Lu, Ling-Hui
Author_xml – sequence: 1
  givenname: Kai-Jian
  surname: Liu
  fullname: Liu, Kai-Jian
  organization: Hunan Univ Sci & Engn, Dept Chem & Bioengn, Yongzhou 425100, Peoples R China
– sequence: 2
  givenname: Zheng
  surname: Wang
  fullname: Wang, Zheng
  organization: Hunan Univ Sci & Engn, Dept Chem & Bioengn, Yongzhou 425100, Peoples R China
– sequence: 3
  givenname: Ling-Hui
  surname: Lu
  fullname: Lu, Ling-Hui
  organization: Hunan Univ Sci & Engn, Dept Chem & Bioengn, Yongzhou 425100, Peoples R China
– sequence: 4
  givenname: Jin-Yang
  orcidid: 0000-0002-8075-9089
  surname: Chen
  fullname: Chen, Jin-Yang
  organization: Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China
– sequence: 5
  givenname: Fei
  surname: Zeng
  fullname: Zeng, Fei
  organization: Hunan Univ Sci & Engn, Dept Chem & Bioengn, Yongzhou 425100, Peoples R China
– sequence: 6
  givenname: Ying-Wu
  orcidid: 0000-0002-2457-0871
  surname: Lin
  fullname: Lin, Ying-Wu
  organization: Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China
– sequence: 7
  givenname: Zhong
  orcidid: 0000-0001-8521-2552
  surname: Cao
  fullname: Cao, Zhong
  organization: Changsha Univ Sci & Technol, Hunan Prov Key Lab Mat Protect Elect Power & Duns, Changsha 410114, Peoples R China
– sequence: 8
  givenname: Xianyong
  surname: Yu
  fullname: Yu, Xianyong
  organization: Hunan Univ Sci & Technol, Sch Chem & Chem Engn, Xiangtan 411201, Peoples R China
– sequence: 9
  givenname: Wei-Min
  orcidid: 0000-0002-9481-6697
  surname: He
  fullname: He, Wei-Min
  email: weiminhe2016@yeah.net
  organization: Hunan Univ Sci & Engn, Dept Chem & Bioengn, Yongzhou 425100, Peoples R China
BookMark eNqNkM9O3DAQh60KpMLSS5_AUi-gKsX_4iRHFJWChOAAnCOvPckaee2t7bDdF-pz1iyoB05cZubw_b4ZzTE68MEDQl8p-UEJ784NmTRhUvLVJ3REheRVxxpy8H-W7DM6TumJEEobKY7Q3_udhzjZlK3GOoQNRJXtM2AYR9AZhxH3l_z-jt0qrLzBS5tOWbWcc_izg7zaubNSIeIctiqahBO4EnsRFGACX2TBv1jS7EZrIOGtzSu8DgWbnYpvGJ69KZZnm-zSQeXstMrYxqiM3RtO0OGoXIIvb32BHi9_PvRX1c3dr-v-4qaaWM1zpU3NRd0J1TBVE2hIY0zd1ZQTRZVpqWGiloSPhrKOjUQawVshJOMlAFpwvkCnr95NDL9nSHlY26TBOeUhzGlgdSO44HKPfnuHPoU5-nLdwETTljWyiBfo-yu1hWUYk7bgNQybaNcq7gZCiCRtwcpAeFPo9uN0b_P-N32Yfeb_AF5yoF4
Cites_doi 10.1016/S1872-2067(19)63420-0
10.3390/antiox7090114
10.1016/j.cclet.2019.10.031
10.1016/j.cclet.2019.12.031
10.1016/j.cclet.2019.05.041
10.1039/c9gc00222g
10.1007/s41061-019-0232-9
10.1039/c8gc02766h
10.1039/c9qo01334b
10.1016/j.cclet.2019.06.052
10.1039/c9cc07655g
10.1021/jm401375q
10.1039/d0qo00233j
10.1016/j.cclet.2019.04.033
10.1021/acs.orglett.9b02921
10.1007/s11426-018-9399-2
10.1016/j.cclet.2019.08.002
10.1002/chem.200501144
10.1007/s41061-018-0184-5
10.1039/d0gc00771d
10.1002/asia.201800532
10.6023/cjoc201900002
10.1016/j.cclet.2020.01.036
10.1039/d0gc02091e
10.1039/d0gc00332h
10.2174/1568026615666150915111741
10.1039/d0gc00070a
10.1021/acs.orglett.9b03192
10.1039/c9gc03253c
10.1039/c2gc00027j
10.1016/j.cclet.2019.05.048
10.1039/c7gc01891f
10.1016/j.cclet.2020.02.011
10.1039/c9gc01357a
10.1039/d0gc00009d
10.1021/acssuschemeng.9b02511
10.1016/j.cclet.2019.09.040
10.1039/c9gc01175g
10.1039/c9gc03841h
10.1039/c8np00093j
10.1021/ja037591o
10.1016/j.cclet.2019.09.041
10.1039/d0gc01500h
10.1002/anie.201906080
10.1002/adsc.201900157
10.1039/c9gc03008e
10.1039/c9gc03713f
10.1007/s11426-018-9446-1
10.1021/acscatal.9b04411
10.1039/c9gc04163j
10.1016/S1872-2067(19)63526-6
10.6023/cjoc202000006
10.6023/cjoc202000041
10.1039/d0gc00383b
ContentType Journal Article
Copyright Copyright Royal Society of Chemistry 2021
Copyright_xml – notice: Copyright Royal Society of Chemistry 2021
DBID 17B
1KN
BLEPL
DTL
EGQ
HGBXW
7SR
7ST
7U6
8BQ
8FD
C1K
JG9
7S9
L.6
DOI 10.1039/d0gc02663h
DatabaseName Web of Knowledge
Current Chemical Reactions
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Web of Science - Science Citation Index Expanded - 2021
Engineered Materials Abstracts
Environment Abstracts
Sustainability Science Abstracts
METADEX
Technology Research Database
Environmental Sciences and Pollution Management
Materials Research Database
AGRICOLA
AGRICOLA - Academic
DatabaseTitle Web of Science
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
Sustainability Science Abstracts
Environment Abstracts
METADEX
Environmental Sciences and Pollution Management
AGRICOLA
AGRICOLA - Academic
DatabaseTitleList AGRICOLA
Web of Science
Materials Research Database
Database_xml – sequence: 1
  dbid: 1KN
  name: Current Chemical Reactions
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Engineering
Chemistry
Environmental Sciences
EISSN 1463-9270
EndPage 500
ExternalDocumentID 000608623000037
GrantInformation_xml – fundername: Hunan Provincial Natural Science Foundation of China; Natural Science Foundation of Hunan Province
  grantid: 2019JJ40090; 2019JJ20008
GroupedDBID 0-7
0R~
17B
1KN
29I
4.4
5GY
705
70~
7~J
AAEMU
AAHBH
AAIWI
AAJAE
AAMEH
AANOJ
AAWGC
AAXHV
AAXPP
ABASK
ABDVN
ABEMK
ABJNI
ABPDG
ABRYZ
ABXOH
ACGFO
ACGFS
ACIWK
ACLDK
ADMRA
ADSRN
AEFDR
AENEX
AENGV
AESAV
AETIL
AFLYV
AFOGI
AFRAH
AFRDS
AFRZK
AFVBQ
AGEGJ
AGKEF
AGRSR
AHGCF
AKMSF
ALMA_UNASSIGNED_HOLDINGS
ALUYA
ANUXI
APEMP
ASKNT
AUDPV
BLAPV
BLEPL
BSQNT
C6K
COF
CS3
D0L
DTL
DU5
EBS
ECGLT
EE0
EF-
F5P
GGIMP
GNO
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
H13
HZ~
H~N
IDZ
J3I
M4U
N9A
O9-
P2P
R56
R7B
RAOCF
RCNCU
RNS
RPMJG
RRA
RRC
RSCEA
SKA
SLH
VH6
7SR
7ST
7U6
8BQ
8FD
C1K
JG9
7S9
L.6
ID FETCH-LOGICAL-g253t-cd534594a72a50e707dd595130a1ad81d245603fd1292f06d43844623a72ec433
ISICitedReferencesCount 109
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000608623000037
ISSN 1463-9262
1463-9270
IngestDate Fri Jul 11 02:15:53 EDT 2025
Mon Jun 30 11:59:06 EDT 2025
Fri May 30 03:34:28 EDT 2025
Fri Aug 29 16:10:17 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords OXIDATION
QUINOLINE N-OXIDES
SULFOXIDES
ELECTRON-TRANSFER
INDUCED DEOXYGENATIVE C2-SULFONYLATION
AMBIENT
RADICAL CYCLIZATION
SULFONES
QUINOXALIN-2(1H)-ONES
REDUCTIVE MINISCI REACTION
Language English
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-g253t-cd534594a72a50e707dd595130a1ad81d245603fd1292f06d43844623a72ec433
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-8521-2552
0000-0002-8075-9089
0000-0002-2457-0871
0000-0002-9481-6697
PQID 2478603662
PQPubID 2047490
PageCount 5
ParticipantIDs proquest_miscellaneous_2574343643
webofscience_primary_000608623000037
webofscience_primary_000608623000037CitationCount
proquest_journals_2478603662
PublicationCentury 2000
PublicationDate 2021-01-07
PublicationDateYYYYMMDD 2021-01-07
PublicationDate_xml – month: 01
  year: 2021
  text: 2021-01-07
  day: 07
PublicationDecade 2020
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
– name: Cambridge
PublicationTitle Green chemistry : an international journal and green chemistry resource : GC
PublicationTitleAbbrev GREEN CHEM
PublicationYear 2021
Publisher Royal Soc Chemistry
Royal Society of Chemistry
Publisher_xml – name: Royal Soc Chemistry
– name: Royal Society of Chemistry
References Huang, BB (WOS:000533979200012) 2020; 22
Xie, LY (WOS:000541151700002) 2020; 41
Gan, ZY (WOS:000533979200028) 2020; 22
Dong, DQ (WOS:000490625200006) 2019; 40
Lu, LH (WOS:000474501100022) 2019; 30
Wang, ZZ (WOS:000490291800003) 2019; 21
Chen, Y (WOS:000456087200007) 2019; 62
Wang, Z (WOS:000518129500030) 2019; 39
Peng, S (WOS:000522786900030) 2020; 40
Lu, LL (WOS:000571356300010) 2020; 22
Li, YM (WOS:000500001300009) 2019; 55
Baciocchi, E (WOS:000187574800054) 2003; 125
Bao, WH (WOS:000506722300045) 2019; 30
Liu, KJ (WOS:000509965500015) 2020; 22
Xie, LY (WOS:000463714600010) 2019; 62
Bao, PL (WOS:000511876900006) 2020; 7
Gong, XX (WOS:000529203600008) 2020; 22
Wang, ZZ (WOS:000506725100018) 2020; 10
Li, GQ (WOS:000482173100040) 2019; 7
Wang, N (WOS:000520977600004) 2020; 37
Peng, S (WOS:000506722300052) 2019; 30
Li, YM (WOS:000480984700001) 2019; 58
Yu, B (WOS:000302018600017) 2012; 14
Mei, YS (WOS:000524318900010) 2020; 22
Cao, Z (WOS:000506722300019) 2019; 30
Shi, JW (WOS:000566823400045) 2020; 40
Lv, YF (WOS:000496489100002) 2019; 21
Feng, MH (WOS:000372847800002) 2016; 16
He, WB (WOS:000548928800035) 2020; 31
Zhu, XJ (WOS:000545862800029) 2020; 22
Chen, SH (WOS:000509965500003) 2020; 22
He, SQ (WOS:000548928800028) 2020; 31
Li, CF (WOS:000544314300019) 2020; 22
Liu, QS (WOS:000464318800005) 2019; 21
Sun, PF (WOS:000413069600007) 2017; 19
Xu, XM (WOS:000509632800006) 2020; 31
Li, GQ (WOS:000467075800014) 2019; 361
Lei, WL (WOS:000453912100005) 2018; 20
Xie, LY (WOS:000475506200013) 2019; 21
Li, GQ (WOS:000489200100053) 2019; 21
Rey, P (WOS:000448393600005) 2018; 7
Han, TH (WOS:000544472100012) 2020; 7
Bonesi, SM (WOS:000238416200014) 2006; 12
Scott, KA (WOS:000426497900005) 2018; 376
Cheng, Z (WOS:000497259500013) 2019; 21
Jia, T (WOS:000458466400001) 2019; 377
Yu, Q (WOS:000471798100019) 2019; 21
Wang, LL (WOS:000509632800010) 2020; 31
Ilardi, EA (WOS:000334572000002) 2014; 57
Liu, KJ (WOS:000506722300056) 2019; 30
Zhang, TS (WOS:000545862800019) 2020; 22
Liu, KJ (WOS:000548928800029) 2020; 31
Wang, YH (WOS:000443679400007) 2018; 13
Mi, X (WOS:000506722300054) 2019; 30
References_xml – volume: 40
  start-page: 1494
  year: 2019
  ident: WOS:000490625200006
  article-title: Visible-light-induced deoxygenative C2-sulfonylation of quinoline N-oxides with sulfinic acids for the synthesis of 2-sulfonylquinoline via radical reactions
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(19)63420-0
– volume: 7
  start-page: ARTN 114
  year: 2018
  ident: WOS:000448393600005
  article-title: Physiological Roles of Plant Methionine Sulfoxide Reductases in Redox Homeostasis and Signaling
  publication-title: ANTIOXIDANTS
  doi: 10.3390/antiox7090114
– volume: 30
  start-page: 2304
  year: 2019
  ident: WOS:000506722300056
  article-title: Solvent-dependent selective oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid under neat conditions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.10.031
– volume: 31
  start-page: 1863
  year: 2020
  ident: WOS:000548928800028
  article-title: Visible-light-promoted oxidative decarboxylation of arylacetic acids in air: Metal-free synthesis of aldehydes and ketones at room temperature
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.12.031
– volume: 31
  start-page: 67
  year: 2020
  ident: WOS:000509632800010
  article-title: Metal-free visible-light-induced oxidative cyclization reaction of 1,6-enynes and arylsulfinic acids leading to sulfonylated benzofurans
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.05.041
– volume: 21
  start-page: 1609
  year: 2019
  ident: WOS:000464318800005
  article-title: Catalyst-free visible-light-initiated oxidative coupling of aryldiazo sulfones with thiols leading to unsymmetrical sulfoxides in air
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc00222g
– volume: 377
  start-page: ARTN 8
  year: 2019
  ident: WOS:000458466400001
  article-title: Chiral Sulfoxide Ligands in Asymmetric Catalysis
  publication-title: TOPICS IN CURRENT CHEMISTRY
  doi: 10.1007/s41061-019-0232-9
– volume: 20
  start-page: 5479
  year: 2018
  ident: WOS:000453912100005
  article-title: Visible-light-enabled aerobic synthesis of benzoin bis-ethers from alkynes and alcohols
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c8gc02766h
– volume: 7
  start-page: 492
  year: 2020
  ident: WOS:000511876900006
  article-title: Visible-light-promoted acridine red catalyzed aerobic oxidative decarboxylative acylation of alpha-oxo-carboxylic acids with quinoxalin-2(1H)-ones
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c9qo01334b
– volume: 30
  start-page: 2259
  year: 2019
  ident: WOS:000506722300045
  article-title: Clean preparation of S-thiocarbamates with in situ generated hydroxide in 2-methyltetrahydrofuran
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.06.052
– volume: 55
  start-page: 14299
  year: 2019
  ident: WOS:000500001300009
  article-title: Visible-light-promoted oxidative halogenation of alkynes
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c9cc07655g
– volume: 57
  start-page: 2832
  year: 2014
  ident: WOS:000334572000002
  article-title: Data-Mining for Sulfur and Fluorine: An Evaluation of Pharmaceuticals To Reveal Opportunities for Drug Design and Discovery
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm401375q
– volume: 7
  start-page: 1671
  year: 2020
  ident: WOS:000544472100012
  article-title: Aerobic C(sp(3))-H oxidation and oxygenation of quaternarized quinolines and pyridines by visible-light-induced photocatalysis
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/d0qo00233j
– volume: 30
  start-page: 1237
  year: 2019
  ident: WOS:000474501100022
  article-title: Sustainable routes for quantitative green selenocyanation of activated alkynes
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.04.033
– volume: 21
  start-page: 7938
  year: 2019
  ident: WOS:000489200100053
  article-title: Photocatalyst-Free Visible-Light-Promoted C(sp(2))-S Coupling: A Strategy for the Preparation of S-Aryl Dithiocarbamates
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b02921
– volume: 62
  start-page: 24
  year: 2019
  ident: WOS:000456087200007
  article-title: Visible light-driven organic photochemical synthesis in China
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-018-9399-2
– volume: 30
  start-page: 2287
  year: 2019
  ident: WOS:000506722300052
  article-title: TsCl-promoted sulfonylation of quinoline N-oxides with sodium sulfinates in water
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.08.002
– volume: 12
  start-page: 4844
  year: 2006
  ident: WOS:000238416200014
  article-title: Photosensitized oxidation of sulfides: Discriminating between the singlet-oxygen mechanism and electron transfer involving superoxide anion or molecular oxygen
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200501144
– volume: 376
  start-page: ARTN 5
  year: 2018
  ident: WOS:000426497900005
  article-title: Analysis of US FDA-Approved Drugs Containing Sulfur Atoms
  publication-title: TOPICS IN CURRENT CHEMISTRY
  doi: 10.1007/s41061-018-0184-5
– volume: 22
  start-page: 4259
  year: 2020
  ident: WOS:000545862800019
  article-title: Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc00771d
– volume: 13
  start-page: 2208
  year: 2018
  ident: WOS:000443679400007
  article-title: Sulfur-Center-Involved Photocatalyzed Reactions
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.201800532
– volume: 39
  start-page: 3594
  year: 2019
  ident: WOS:000518129500030
  article-title: Radical Cyclization Strategy towards Indolo[1,2-a]quinolines
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc201900002
– volume: 31
  start-page: 1868
  year: 2020
  ident: WOS:000548928800029
  article-title: 1,2-Diethoxyethane catalyzed oxidative cleavage of gem-disubstituted aromatic alkenes to ketones under minimal solvent conditions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2020.01.036
– volume: 22
  start-page: 5989
  year: 2020
  ident: WOS:000571356300010
  article-title: Visible-light-promoted oxidative halogenation of (hetero)arenes
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc02091e
– volume: 22
  start-page: 1906
  year: 2020
  ident: WOS:000529203600008
  article-title: A metal-free route to alkynyl sulfones under photoinduced conditions with the insertion of sulfur dioxide
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc00332h
– volume: 16
  start-page: 1200
  year: 2016
  ident: WOS:000372847800002
  article-title: Sulfur Containing Scaffolds in Drugs: Synthesis and Application in Medicinal Chemistry
  publication-title: CURRENT TOPICS IN MEDICINAL CHEMISTRY
  doi: 10.2174/1568026615666150915111741
– volume: 22
  start-page: 2956
  year: 2020
  ident: WOS:000533979200028
  article-title: Visible-light-promoted oxidative desulphurisation: a strategy for the preparation of unsymmetrical ureas from isothiocyanates and amines using molecular oxygen
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc00070a
– volume: 21
  start-page: 8925
  year: 2019
  ident: WOS:000497259500013
  article-title: Switchable Synthesis of Aryl Sulfones and Sulfoxides through Solvent-Promoted Oxidation of Sulfides with O-2/Air
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b03192
– volume: 21
  start-page: 6051
  year: 2019
  ident: WOS:000496489100002
  article-title: Visible-light-mediated metal-free decarboxylative acylations of isocyanides with alpha-oxocarboxylic acids and water leading to alpha-ketoamides
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03253c
– volume: 14
  start-page: 957
  year: 2012
  ident: WOS:000302018600017
  article-title: Catalyst-free approach for solvent-dependent selective oxidation of organic sulfides with oxone
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c2gc00027j
– volume: 31
  start-page: 49
  year: 2020
  ident: WOS:000509632800006
  article-title: Recent advances in sulfenylation of C(sp(3))-H bond under transition metal-free conditions
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.05.048
– volume: 19
  start-page: 4785
  year: 2017
  ident: WOS:000413069600007
  article-title: Visible light-induced C-H sulfenylation using sulfinic acids
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c7gc01891f
– volume: 31
  start-page: 1895
  year: 2020
  ident: WOS:000548928800035
  article-title: Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2020.02.011
– volume: 21
  start-page: 3436
  year: 2019
  ident: WOS:000471798100019
  article-title: Ambient and aerobic carbon-carbon bond cleavage toward alpha-ketoester synthesis by transition-metal-free photocatalysis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc01357a
– volume: 22
  start-page: 2270
  year: 2020
  ident: WOS:000524318900010
  article-title: Synthesis of sulfone-functionalized chroman-4-ones and chromans through visible-light-induced cascade radical cyclization under transition-metal-free conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc00009d
– volume: 7
  start-page: 14009
  year: 2019
  ident: WOS:000482173100040
  article-title: Photocatalyst-Free Regioselective C-H Thiocyanation of 4-Anilinocoumarins under Visible Light
  publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING
  doi: 10.1021/acssuschemeng.9b02511
– volume: 30
  start-page: 2295
  year: 2019
  ident: WOS:000506722300054
  article-title: Visible-light-promoted sulfonylmethylation of imidazopyridines
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.09.040
– volume: 21
  start-page: 3858
  year: 2019
  ident: WOS:000475506200013
  article-title: Visible-light-induced deoxygenative C2-sulfonylation of quinoline N-oxides with sulfinic acids
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc01175g
– volume: 22
  start-page: 322
  year: 2020
  ident: WOS:000509965500003
  article-title: General sulfone construction via sulfur dioxide surrogate control
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03841h
– volume: 37
  start-page: 246
  year: 2020
  ident: WOS:000520977600004
  article-title: Construction of sulfur-containing moieties in the total synthesis of natural products
  publication-title: NATURAL PRODUCT REPORTS
  doi: 10.1039/c8np00093j
– volume: 125
  start-page: 16444
  year: 2003
  ident: WOS:000187574800054
  article-title: Electron transfer and singlet oxygen mechanisms in the photooxygenation of dibutyl sulfide and thioanisole in MeCN sensitized by N-methylquinolinium tetrafluoborate and 9,10-dicyanoanthracene. The probable involvement of a thiadioxirane intermediate in electron transfer photooxygenations
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja037591o
– volume: 30
  start-page: 2132
  year: 2019
  ident: WOS:000506722300019
  article-title: The concept of dual roles design in clean organic preparation
  publication-title: CHINESE CHEMICAL LETTERS
  doi: 10.1016/j.cclet.2019.09.041
– volume: 22
  start-page: 3896
  year: 2020
  ident: WOS:000544314300019
  article-title: Selectivity switch in the aerobic oxygenation of sulfides photocatalysed by visible-light-responsive decavanadate
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc01500h
– volume: 58
  start-page: 13499
  year: 2019
  ident: WOS:000480984700001
  article-title: Selective Late-Stage Oxygenation of Sulfides with Ground-State Oxygen by Uranyl Photocatalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201906080
– volume: 361
  start-page: 1808
  year: 2019
  ident: WOS:000467075800014
  article-title: Metal-Free Synthesis of Thiosulfonates via Insertion of Sulfur Dioxide
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201900157
– volume: 21
  start-page: 5512
  year: 2019
  ident: WOS:000490291800003
  article-title: Visible-light-mediated photoredox decarbonylative Minisci-type alkylation with aldehydes under ambient air conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03008e
– volume: 22
  start-page: 433
  year: 2020
  ident: WOS:000509965500015
  article-title: Selective oxidation of (hetero)sulfides with molecular oxygen under clean conditions
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc03713f
– volume: 62
  start-page: 460
  year: 2019
  ident: WOS:000463714600010
  article-title: Metal-free C3-alkoxycarbonylation of quinoxalin-2(1H)-ones with carbazates as ecofriendly ester sources
  publication-title: SCIENCE CHINA-CHEMISTRY
  doi: 10.1007/s11426-018-9446-1
– volume: 10
  start-page: 154
  year: 2020
  ident: WOS:000506725100018
  article-title: Bromide-Promoted Visible-Light-Induced Reductive Minisci Reaction with Aldehydes
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04411
– volume: 22
  start-page: 2804
  year: 2020
  ident: WOS:000533979200012
  article-title: Three-component aminoselenation of alkenes via visible-light enabled Fe-catalysis
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c9gc04163j
– volume: 41
  start-page: 1168
  year: 2020
  ident: WOS:000541151700002
  article-title: C(sp(2))-H/O-H cross-dehydrogenative coupling of quinoxalin-2(1H)-ones with alcohols under visible-light photoredox catalysis
  publication-title: CHINESE JOURNAL OF CATALYSIS
  doi: 10.1016/S1872-2067(19)63526-6
– volume: 40
  start-page: 541
  year: 2020
  ident: WOS:000522786900030
  article-title: Visible Light-Induced Aldehyde Reductive Minisci Reaction towards N-Heterocycles
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc202000006
– volume: 40
  start-page: 2170
  year: 2020
  ident: WOS:000566823400045
  article-title: External Photocatalyst-Free Visible-Light-Induced C3-Acylation of Quinoxalin-2(1H)-ones
  publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.6023/cjoc202000041
– volume: 22
  start-page: 4357
  year: 2020
  ident: WOS:000545862800029
  article-title: Light and oxygen-enabled sodium trifluoromethanesulfinate-mediated selective oxidation of C-H bonds
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/d0gc00383b
SSID ssj0011764
Score 2.6113625
Snippet A safe, practical and eco-friendly method for the switchable synthesis of sulfoxides and sulfones through visible-light-initiated oxygenation of sulfides at...
Source Web of Science
SourceID proquest
webofscience
SourceType Aggregation Database
Enrichment Source
Index Database
StartPage 496
SubjectTerms Additives
Ambient temperature
Chemistry
Chemistry, Multidisciplinary
Green & Sustainable Science & Technology
Green chemistry
Irradiation
light
Light irradiation
Oxygen
Oxygenation
Physical Sciences
Radiation
Science & Technology
Science & Technology - Other Topics
solvents
Sulfides
Sulfones
sulfoxides
Transition metals
Title Synergistic cooperative effect of CF3SO2Na and bis(2-butoxyethyl)ether towards selective oxygenation of sulfides with molecular oxygen under visible-light irradiation
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000608623000037
https://www.proquest.com/docview/2478603662
https://www.proquest.com/docview/2574343643
Volume 23
WOS 000608623000037
WOSCitedRecordID wos000608623000037
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbhMxELZCewAOCAIVgYKMVCTQysVre_-OVZQQqpIemorCJdpdO2mkkFTJrkQ5lrfhsXrjLRh7vT-BHgpStFrtjh1L8609M575jNAeS1zJJoITzjxFBFcpSaRISOrGQmmCqzTRcciPQ39wKg7PvLNW61cjaynPkv30-411Jf-jVXgGetVVsv-g2apTeAD3oF-4gobheisdn1zqyj1Dteyky-WFsjTeRZKGybTom2wG-PGT4_KWDU0hlpNofgEwfZM8W367VKCy-WsWmQpgMEl1Ou3aWZtzcnSnIAIDqSzMdT6fzKSy1XFfy1N2rZg5Xnfl6Mr1ZK7IXIcAnNlqpZkQKihYm9ik_jhpefKcCVLEC0NkUccqS4YLPe7pHw1WdgvCtHxfc0nO8iJfZEYOGx_BJxsh_3Ku7KqtZXMboJiSQT6rcx5s6cpsQT7HVtqGSJhrQiRBY1YXPicRK04oKaf9osy5hLdzsS8in3iUNmZzEfkNw8C--2vNoVxTtko6TcGf9fl5vbKW2QTD43H_9OhoPOqdje6gbQYeDUzJ2we90YejasvLDQzXWTXWkkuXR-_qvjf8oBssJWMVjR6iB9adwQcFNh-hllq00d1uqZo2ut8gvGyjnV5dVwnN7MKyfox-NqCMG1DGBZTxcoK7_eurHyfH11dXwxgDDDDA980GeN8a6GILXVxBFzegq3sqoYs1dHEFXSuGDXTxBnRxA7pP0Gm_N-oOiD1GhEyZxzOSSo8LLxJxwGKPqoAGUnrgWHAau7EEf03v_VM-kWD6sgn1peChEOAWQAOVCs530NZiuVBPEQbrXlIq44gymNBUkASeH6YilIyGsUtFB-2W6hnb72I9ZiIIoX_fZx30qnoNatBbc_FCLXOQ8QJd4g3uQQftNdU6vihIZ8aGOSmEUVHDGdVB7m3EupboXxNcZM9u8ffP0b36C9pFW9kqVy_A7M6SlxawvwHFjeKx
linkProvider Royal Society of Chemistry
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Synergistic+cooperative+effect+of+CF%E2%82%83SO%E2%82%82Na+and+bis%282-butoxyethyl%29ether+towards+selective+oxygenation+of+sulfides+with+molecular+oxygen+under+visible-light+irradiation&rft.jtitle=Green+chemistry+%3A+an+international+journal+and+green+chemistry+resource+%3A+GC&rft.au=Liu%2C+Kai-Jian&rft.au=Wang%2C+Zheng&rft.au=Lu%2C+Ling-Hui&rft.au=Chen%2C+Jin-Yang&rft.date=2021-01-07&rft.issn=1463-9270&rft.volume=23&rft.issue=1+p.496-500&rft.spage=496&rft.epage=500&rft_id=info:doi/10.1039%2Fd0gc02663h&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1463-9262&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1463-9262&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1463-9262&client=summon