The triple role of rongalite in aminosulfonylation of aryldiazonium tetrafluoroborates: synthesis of N-aminosulfonamides via a radical coupling reaction
A simple and convenient method for N-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free, oxidant-free, and room-temperature conditions is reported. This method does not require an external amine source, with the aryldiazonium tetrafl...
Saved in:
| Published in | Chemical communications (Cambridge, England) Vol. 54; no. 55; pp. 7641 - 7644 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
CAMBRIDGE
Royal Soc Chemistry
2018
Royal Society of Chemistry |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | A simple and convenient method for N-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free, oxidant-free, and room-temperature conditions is reported. This method does not require an external amine source, with the aryldiazonium tetrafluoroborates participating as both an aryl radical and a potential amine source in the transformation. Mechanistic studies revealed that rongalite could act as a radical initiator, a sulfur dioxide surrogate and a reducing reagent simultaneously in this reaction. |
|---|---|
| AbstractList | A simple and convenient method for
N
-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free, oxidant-free, and room-temperature conditions is reported. This method does not require an external amine source, with the aryldiazonium tetrafluoroborates participating as both an aryl radical and a potential amine source in the transformation. Mechanistic studies revealed that rongalite could act as a radical initiator, a sulfur dioxide surrogate and a reducing reagent simultaneously in this reaction. A simple and convenient method for N-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free, oxidant-free, and room-temperature conditions is reported. This method does not require an external amine source, with the aryldiazonium tetrafluoroborates participating as both an aryl radical and a potential amine source in the transformation. Mechanistic studies revealed that rongalite could act as a radical initiator, a sulfur dioxide surrogate and a reducing reagent simultaneously in this reaction. |
| Author | Wang, Miao Xiang, Jia-Chen Huang, Ping-Ping Wang, Jun-Gang Guo, Wu-Yinzheng Wu, An-Xin Wu, Yan-Dong Tang, Bo-Cheng Guan, Ao-Yu |
| Author_xml | – sequence: 1 givenname: Miao surname: Wang fullname: Wang, Miao organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 2 givenname: Bo-Cheng surname: Tang fullname: Tang, Bo-Cheng organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 3 givenname: Jun-Gang surname: Wang fullname: Wang, Jun-Gang organization: Guizhou Minzu Univ, Sch Chem Engn, Guiyang 550025, Guizhou, Peoples R China – sequence: 4 givenname: Jia-Chen orcidid: 0000-0003-2422-6103 surname: Xiang fullname: Xiang, Jia-Chen organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 5 givenname: Ao-Yu surname: Guan fullname: Guan, Ao-Yu organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 6 givenname: Ping-Ping surname: Huang fullname: Huang, Ping-Ping organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 7 givenname: Wu-Yinzheng surname: Guo fullname: Guo, Wu-Yinzheng organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 8 givenname: Yan-Dong surname: Wu fullname: Wu, Yan-Dong organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China – sequence: 9 givenname: An-Xin surname: Wu fullname: Wu, An-Xin email: chwuax@mail.ccnu.edu.cn organization: Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Hubei, Peoples R China |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29931018$$D View this record in MEDLINE/PubMed |
| BookMark | eNqN0c1uFSEUB3BiauyHbnwAQ-LGaEZhgBnozky0mjS6qYm7CcMcbmm4cAVGc30SH1emtzbGlSw4Z_HL4YT_KToKMQBCTyl5TQlTb4w0hrC-l5sH6ISyjjeCy69Hay9U0zMujtFpzjekHirkI3TcKsUoofIE_bq6BlyS23nAKdYr2lrDRntXALuA9daFmBdvY9h7XVwMK9Fp72enf8bgli0uUJK2fokpTjHpAvkc530o15BdXvmn5q8xtZ0h4-9OY42Tnp3RHpu47LwLG5xAm_WVx-ih1T7Dk7t6hr68f3c1fGguP198HN5eNoZRURqlQEkgdhK8t4IDZZZD14OFTrVTZ4khnbKcU0slUy3pjZaaCSnambZMTOwMvTjM3aX4bYFcxq3LBrzXAeKSx5ZUTLggrNLn_9CbuKRQt6uq41QpwWhVLw_KpJhzAjvuktvWDxspGde8xkEOw21eFxU_uxu5TFuY7-mfgCp4dQA_YIo2GwfBwD2rgXLeUirlGm1Xtfx_Pbhym-cQl1DYbxzQteA |
| CitedBy_id | crossref_primary_10_1021_acs_orglett_1c03877 crossref_primary_10_1039_D0OB01718C crossref_primary_10_1002_slct_202002878 crossref_primary_10_1055_a_2059_3168 crossref_primary_10_1021_acs_joc_2c00936 crossref_primary_10_6023_cjoc202305014 crossref_primary_10_1039_D3OB00902E crossref_primary_10_1016_j_cclet_2023_109152 crossref_primary_10_1039_D2RA07807D crossref_primary_10_1039_D3OB01794J crossref_primary_10_1039_C9CC00008A crossref_primary_10_1002_slct_202302672 crossref_primary_10_1021_acs_joc_1c03031 crossref_primary_10_1016_j_jfluchem_2020_109653 crossref_primary_10_1002_asia_202200408 crossref_primary_10_1039_C8QO00965A crossref_primary_10_1002_cjoc_202300342 crossref_primary_10_1016_j_cclet_2020_04_043 crossref_primary_10_1039_D2OB00665K crossref_primary_10_1021_acs_orglett_4c01364 crossref_primary_10_1002_slct_202302903 crossref_primary_10_1039_D1OB02284A crossref_primary_10_1002_adsc_201801445 crossref_primary_10_1039_C8CC07599A crossref_primary_10_1021_acs_orglett_3c02839 crossref_primary_10_1039_D0CC05800A crossref_primary_10_1016_j_tetlet_2019_151539 crossref_primary_10_1021_acs_orglett_8b03718 crossref_primary_10_1021_acs_orglett_9b03212 crossref_primary_10_1039_D0SC02947E crossref_primary_10_1021_acs_chemrev_0c01030 crossref_primary_10_1016_j_fuel_2021_122430 crossref_primary_10_1039_C8QO00824H crossref_primary_10_1021_acs_orglett_0c00823 crossref_primary_10_1021_acs_orglett_4c00849 crossref_primary_10_1002_zaac_202200087 crossref_primary_10_1002_cjoc_201900505 crossref_primary_10_1039_C9CC03789F crossref_primary_10_1039_D2GC00910B crossref_primary_10_1039_D3RA03123C crossref_primary_10_1002_cjoc_202300751 crossref_primary_10_1039_C8CC07434H crossref_primary_10_1039_C8QO01048J crossref_primary_10_1021_acs_joc_9b01113 |
| Cites_doi | 10.1039/c3ob40997j 10.1021/cr100175t 10.3389/fpls.2012.00245 10.1021/jf203772d 10.1002/anie.201409283 10.1002/anie.201508370 10.1039/b315580c 10.1021/ja405949a 10.1021/acs.orglett.6b02894 10.1517/13543776.2013.742065 10.1039/c7qo01073g 10.1021/acs.joc.7b00140 10.1039/c5cc09830k 10.1016/j.tet.2008.09.022 10.1021/ol201957n 10.1002/ajoc.201500103 10.1021/acs.orglett.5b01540 10.1039/c4ob01727g 10.1021/ol0268743 10.1021/ol4010454 10.1021/ol5018849 10.1016/j.ejmech.2007.01.012 10.1039/c6qo00060f 10.1021/jm100398z 10.1021/acs.orglett.5b03545 10.1039/c4ob02139h 10.1021/jm0494974 10.1002/anie.201309851 10.1039/c7qo00127d 10.1039/c4cc03032j 10.1039/c4cc05401f 10.1039/c2cc34957d 10.1021/acs.orglett.5b03552 10.1055/s-0035-1560444 10.1021/acs.orglett.8b00093 10.1021/ja1081124 10.1039/c2cc33725h 10.1002/adsc.201700501 10.1021/jm031117b 10.1039/C6QO00060F 10.1039/C4CC05401F 10.1039/C4OB02139H 10.1039/C7QO00127D 10.1039/C4OB01727G 10.1055/s-1986-31803 10.1039/B315580C 10.1039/C4CC03032J 10.1039/C7QO01073G 10.1007/978-981-10-4202-7 10.1126/science.287.5460.1960 10.1016/j.bmc.2015.02.026 10.1039/C5CC09830K |
| ContentType | Journal Article |
| Copyright | Copyright Royal Society of Chemistry 2018 |
| Copyright_xml | – notice: Copyright Royal Society of Chemistry 2018 |
| DBID | 1KM 1KN 95M AFRED BLEPL DTL HBEAY NPM AAYXX CITATION 7SR 7U5 8BQ 8FD JG9 L7M 7X8 |
| DOI | 10.1039/c8cc03778g |
| DatabaseName | Index Chemicus Current Chemical Reactions Conference Proceedings Citation Index - Science (CPCI-S) Conference Proceedings Citation Index - Science (CPCI-S) 2018 Web of Science Core Collection Science Citation Index Expanded Web of Science - Science Citation Index Expanded - 2018 PubMed CrossRef Engineered Materials Abstracts Solid State and Superconductivity Abstracts METADEX Technology Research Database Materials Research Database Advanced Technologies Database with Aerospace MEDLINE - Academic |
| DatabaseTitle | Web of Science PubMed CrossRef Materials Research Database Engineered Materials Abstracts Solid State and Superconductivity Abstracts Technology Research Database Advanced Technologies Database with Aerospace METADEX MEDLINE - Academic |
| DatabaseTitleList | CrossRef Materials Research Database Web of Science PubMed MEDLINE - Academic |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 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 | Chemistry |
| EISSN | 1364-548X |
| EndPage | 7644 |
| ExternalDocumentID | 10_1039_C8CC03778G 29931018 000442118800016 |
| Genre | Journal Article |
| GrantInformation_xml | – fundername: Fundamental Research Funds for the Central Universities grantid: CCNU15ZX002; CCNU16A05002 – fundername: 111 Project; Ministry of Education, China - 111 Project grantid: B17019 – fundername: Hubei Provincial Natural Science Foundation of China; National Natural Science Foundation of China (NSFC) grantid: 2017CFB355 – fundername: National Natural Science Foundation of China; National Natural Science Foundation of China (NSFC) grantid: 21472056; 21602070; 21772051 |
| GroupedDBID | --- -DZ -JG -~X 0-7 0R~ 1KM 1KN 29B 2WC 4.4 53G 5GY 6J9 705 70~ 7~J 95M AAEMU AAHBH AAIWI AAJAE AAMEH AANOJ AAWGC AAXHV AAXPP ABASK ABDVN ABEMK ABJNI ABPDG ABRYZ ABXOH ACBEA ACGFO ACGFS ACIWK ACLDK ACNCT ADMRA ADSRN AEFDR AENEX AENGV AESAV AETIL AFLYV AFOGI AFRDS AFRED AFVBQ AGEGJ AGKEF AGRSR AGSTE AHGCF ALMA_UNASSIGNED_HOLDINGS ANUXI APEMP ASKNT AUDPV AZFZN BLAPV BLEPL BSQNT C6K CS3 DTL DU5 EBS ECGLT EE0 EF- EJD F5P GGIMP GNO GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED H13 HZ~ H~N IDZ IH2 J3I M4U N9A O9- P2P R7B R7C R7D RAOCF RCNCU RIG RPMJG RRA RRC RSCEA SJN SKA SKF SKH SLH TN5 TWZ UPT VH6 VQA WH7 X7L NPM 0UZ 186 1TJ 3EH 6TJ 71~ 9M8 AAYOK AAYXX ACHDF ACMRT AFFNX AHGXI AI. ANBJS ANLMG ASPBG AVWKF BBWZM CAG CITATION COF EEHRC F20 FA8 FEDTE HVGLF IDY J3G J3H KC5 L-8 MVM NDZJH OHT R56 RCLXC RNS ROL RRXOS UHB VH1 WHG XJT ZCG ZKB 7SR 7U5 8BQ 8FD JG9 L7M 7X8 |
| ID | FETCH-LOGICAL-c315t-99e98e0fb547f54e13f4e67efe692b6f0c069f441f1839207ca8a35852d1235b3 |
| ISICitedReferencesCount | 45 |
| ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000442118800016 |
| ISSN | 1359-7345 |
| IngestDate | Fri Aug 16 23:20:32 EDT 2024 Thu Oct 10 15:57:36 EDT 2024 Fri Aug 23 01:48:49 EDT 2024 Wed Oct 16 00:58:22 EDT 2024 Tue Aug 27 15:37:53 EDT 2024 Fri Nov 08 20:07:16 EST 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 55 |
| Keywords | INSERTION DABCO-CENTER-DOT(SO2) REAGENTS SULFUR-DIOXIDE ONE-POT SULFONAMIDES GENERATION DABSO DERIVATIVES FIXATION |
| Language | English |
| LinkModel | OpenURL |
| LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
| MergedId | FETCHMERGED-LOGICAL-c315t-99e98e0fb547f54e13f4e67efe692b6f0c069f441f1839207ca8a35852d1235b3 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ORCID | 0000-0003-2422-6103 0000-0001-7673-210X |
| PMID | 29931018 |
| PQID | 2064199531 |
| PQPubID | 2047502 |
| PageCount | 4 |
| ParticipantIDs | proquest_journals_2064199531 proquest_miscellaneous_2058504503 webofscience_primary_000442118800016 webofscience_primary_000442118800016CitationCount pubmed_primary_29931018 crossref_primary_10_1039_C8CC03778G |
| PublicationCentury | 2000 |
| PublicationDate | 2018-00-00 |
| PublicationDateYYYYMMDD | 2018-01-01 |
| PublicationDate_xml | – year: 2018 text: 2018-00-00 |
| PublicationDecade | 2010 |
| PublicationPlace | CAMBRIDGE |
| PublicationPlace_xml | – name: CAMBRIDGE – name: England – name: Cambridge |
| PublicationTitle | Chemical communications (Cambridge, England) |
| PublicationTitleAbbrev | CHEM COMMUN |
| PublicationTitleAlternate | Chem Commun (Camb) |
| PublicationYear | 2018 |
| Publisher | Royal Soc Chemistry Royal Society of Chemistry |
| Publisher_xml | – name: Royal Soc Chemistry – name: Royal Society of Chemistry |
| References | Deeming, AS (WOS:000368069200052) 2016; 55 Noutoshi, Y (WOS:000208837900241) 2012; 3 Harrak, Y (WOS:000281753700004) 2010; 53 Kleeman, A. (000442118800016.22) 1999 Jiang, J (WOS:000398986000027) 2017; 82 Tsai, AS (WOS:000369771800042) 2016; 18 (000442118800016.3) 1983 Waldmann, C (WOS:000320979000017) 2013; 15 Liu, NW (WOS:000380250800005) 2016; 48 Crowley, PJ (WOS:000179173700035) 2002; 4 Banerjee, M (WOS:000226591700024) 2005; 48 Zhang, F (WOS:000426013600068) 2018; 20 Bartholow, M. (000442118800016.7) 1000 Bisseret, P (WOS:000323141800001) 2013; 11 Zhang, WX (WOS:000369641300026) 2016; 52 Nguyen, B (WOS:000284792000025) 2010; 132 Deeming, AS (WOS:000348372900015) 2015; 54 An, YY (WOS:000342069600031) 2014; 50 Mariusz, M. (000442118800016.28) 2015; 23 Dominique, G. (000442118800016.15) 2004; 47 Hamada, T. (000442118800016.19) 1986 Liu, G (WOS:000349032400001) 2015; 13 Zheng, D. (000442118800016.49) 2017 Drews, J (WOS:000085902800046) 2000; 287 Emmett, EJ (WOS:000357386200001) 2015; 4 Ye, SQ (WOS:000308653800026) 2012; 48 Wang, M (WOS:000369771800046) 2016; 18 Scozzafava, A (WOS:000313676400005) 2013; 23 Liu, T (WOS:000407065400018) 2017; 359 Kotha, S (WOS:000301988700010) 2012; 112 Shavnya, A (WOS:000388428600020) 2016; 18 Ye, SQ (WOS:000306176300029) 2012; 48 Colombe, JR (WOS:000356845000078) 2015; 17 Xu, WM (WOS:000300462500024) 2012; 60 Chappell, N. (000442118800016.9) 1921; 37 Woolven, H (WOS:000294703900032) 2011; 13 Ouchi, A (WOS:000220847800006) 2004; 6 Wang, XB (WOS:000339982300053) 2014; 16 Zhou, KD (WOS:000405862600032) 2017; 4 (000442118800016.2) 2004 DeBergh, JR (WOS:000322432400015) 2013; 135 Wang, ZL (WOS:000260844000004) 2008; 64 Qiu, GYS (WOS:000431292400025) 2018; 5 Zheng, DQ (WOS:000339861700016) 2014; 50 Zheng, DQ (WOS:000336834000018) 2014; 53 Smith, DA (WOS:000251872500006) 2008; 11 Fan, H (WOS:000249197600011) 2007; 42 Aziz, J (WOS:000345458700002) 2014; 12 (000442118800016.1) 2008 Li, YW (WOS:000374853900007) 2016; 3 Ye (C8CC03778G-(cit7d)/*[position()=1]) 2012; 48 Zhang (C8CC03778G-(cit10b)/*[position()=1]) 2016; 52 Li (C8CC03778G-(cit7a)/*[position()=1]) 2016; 3 Smith (C8CC03778G-(cit1b)/*[position()=1]) 2008; 11 Zhou (C8CC03778G-(cit6c)/*[position()=1]) 2017; 4 Deeming (C8CC03778G-(cit6f)/*[position()=1]) 2016; 55 Harrak (C8CC03778G-(cit3e)/*[position()=1]) 2010; 53 Jiang (C8CC03778G-(cit12a)/*[position()=1]) 2017; 82 Woolven (C8CC03778G-(cit6e)/*[position()=1]) 2011; 13 Shavnya (C8CC03778G-(cit10a)/*[position()=1]) 2016; 18 Banerjee (C8CC03778G-(cit3d)/*[position()=1]) 2005; 48 Bisseret (C8CC03778G-(cit5a)/*[position()=1]) 2013; 11 Drews (C8CC03778G-(cit2a)/*[position()=1]) 2000; 287 Xu (C8CC03778G-(cit1g)/*[position()=1]) 2012; 60 Zhang (C8CC03778G-(cit6d)/*[position()=1]) 2018; 20 Chappell (C8CC03778G-(cit8c)/*[position()=1]) 1921; 37 Wang (C8CC03778G-(cit11)/*[position()=1]) 2016; 18 Kleeman (C8CC03778G-(cit1h)/*[position()=1]) 1999 Scozzafava (C8CC03778G-(cit3f)/*[position()=1]) 2013; 23 Smith (C8CC03778G-(cit3g)/*[position()=1]) 2008; 11 Bartholow (C8CC03778G-(cit2b)/*[position()=1]) Qiu (C8CC03778G-(cit5e)/*[position()=1]) 2018; 5 Nguyen (C8CC03778G-(cit6a)/*[position()=1]) 2010; 132 Noutoshi (C8CC03778G-(cit1d)/*[position()=1]) 2012; 3 Aziz (C8CC03778G-(cit1f)/*[position()=1]) 2014; 12 Zheng (C8CC03778G-(cit6m)/*[position()=1]) 2014; 50 Dominique (C8CC03778G-(cit3c)/*[position()=1]) 2004; 47 Wang (C8CC03778G-(cit7c)/*[position()=1]) 2014; 16 Ouchi (C8CC03778G-(cit8a)/*[position()=1]) 2004; 6 Fan (C8CC03778G-(cit3b)/*[position()=1]) 2007; 42 DeBergh (C8CC03778G-(cit6g)/*[position()=1]) 2013; 135 Deeming (C8CC03778G-(cit6j)/*[position()=1]) 2015; 54 Waldmann (C8CC03778G-(cit6k)/*[position()=1]) 2013; 15 Tsai (C8CC03778G-(cit6h)/*[position()=1]) 2016; 18 An (C8CC03778G-(cit6l)/*[position()=1]) 2014; 50 Zheng (C8CC03778G-(cit6b)/*[position()=1]) 2014; 53 Liu (C8CC03778G-(cit1e)/*[position()=1]) 2016 Zheng (C8CC03778G-(cit5d)/*[position()=1]) 2017 Hamada (C8CC03778G-(cit4)/*[position()=1]) 1986 Ye (C8CC03778G-(cit7b)/*[position()=1]) 2012; 48 Colombe (C8CC03778G-(cit6i)/*[position()=1]) 2015; 17 Liu (C8CC03778G-(cit12b)/*[position()=1]) 2017; 359 Emmett (C8CC03778G-(cit5c)/*[position()=1]) 2015; 4 Crowley (C8CC03778G-(cit1c)/*[position()=1]) 2002; 4 Harrak (C8CC03778G-(cit1a)/*[position()=1]) 2010; 53 Wang (C8CC03778G-(cit13)/*[position()=1]) 2008; 64 Mariusz (C8CC03778G-(cit3a)/*[position()=1]) 2015; 23 Kotha (C8CC03778G-(cit9)/*[position()=2]) 2012; 112 Liu (C8CC03778G-(cit5b)/*[position()=1]) 2015; 13 |
| References_xml | – volume: 11 start-page: 5393 year: 2013 ident: WOS:000323141800001 article-title: Taming sulfur dioxide: a breakthrough for its wide utilization in chemistry and biology publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c3ob40997j contributor: fullname: Bisseret, P – volume: 37 start-page: 206 year: 1921 ident: 000442118800016.9 publication-title: J. Soc. Dyers Colour contributor: fullname: Chappell, N. – volume: 112 start-page: 1650 year: 2012 ident: WOS:000301988700010 article-title: Rongalite: A Useful Green Reagent in Organic Synthesis publication-title: CHEMICAL REVIEWS doi: 10.1021/cr100175t contributor: fullname: Kotha, S – volume: 3 start-page: ARTN 245 year: 2012 ident: WOS:000208837900241 article-title: Sulfonamides identified as plant immune-priming compounds in high-throughput chemical screening increase disease resistance in Arabidopsis thaliana publication-title: FRONTIERS IN PLANT SCIENCE doi: 10.3389/fpls.2012.00245 contributor: fullname: Noutoshi, Y – volume: 60 start-page: 1036 year: 2012 ident: WOS:000300462500024 article-title: Inhibition of Tobacco Bacterial Wilt with Sulfone Derivatives Containing an 1,3,4-Oxadiazole Moiety publication-title: JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY doi: 10.1021/jf203772d contributor: fullname: Xu, WM – volume: 54 start-page: 1168 year: 2015 ident: WOS:000348372900015 article-title: Combining Organometallic Reagents, the Sulfur Dioxide Surrogate DABSO, and Amines: A One-Pot Preparation of Sulfonamides, Amenable to Array Synthesis publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201409283 contributor: fullname: Deeming, AS – volume: 23 start-page: 1421 year: 2015 ident: 000442118800016.28 publication-title: Bioorg. Med. Chem. contributor: fullname: Mariusz, M. – year: 1999 ident: 000442118800016.22 publication-title: Pharmaceutical Substances: Syntheses, Patents, Applications contributor: fullname: Kleeman, A. – year: 2008 ident: 000442118800016.1 – volume: 55 start-page: 747 year: 2016 ident: WOS:000368069200052 article-title: Palladium(II)-Catalyzed Synthesis of Sulfinates from Boronic Acids and DABSO: A Redox-Neutral, Phosphine-Free Transformation publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201508370 contributor: fullname: Deeming, AS – volume: 6 start-page: 198 year: 2004 ident: WOS:000220847800006 article-title: Reductive total chlorine free photochemical bleaching of cellulosic fabrics, an energy conserving process publication-title: GREEN CHEMISTRY doi: 10.1039/b315580c contributor: fullname: Ouchi, A – volume: 135 start-page: 10638 year: 2013 ident: WOS:000322432400015 article-title: Synthesis of Aryl Sulfonamides via Palladium-Catalyzed Chlorosulfonylation of Arylboronic Acids publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja405949a contributor: fullname: DeBergh, JR – volume: 18 start-page: 5848 year: 2016 ident: WOS:000388428600020 article-title: Reaction of Alkyl Halides with Rongalite: One-Pot and Telescoped Syntheses of Aliphatic Sulfonamides, Sulfonyl Fluorides, and Unsymmetrical Sulfones publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.6b02894 contributor: fullname: Shavnya, A – year: 2017 ident: 000442118800016.49 publication-title: Sulfur Dioxide Insertion Reactions for Organic Synthesis contributor: fullname: Zheng, D. – volume: 23 start-page: 203 year: 2013 ident: WOS:000313676400005 article-title: Secondary and tertiary sulfonamides: a patent review (2008-2012) publication-title: EXPERT OPINION ON THERAPEUTIC PATENTS doi: 10.1517/13543776.2013.742065 contributor: fullname: Scozzafava, A – volume: 5 start-page: 691 year: 2018 ident: WOS:000431292400025 article-title: Insertion of sulfur dioxide via a radical process: an efficient route to sulfonyl compounds publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c7qo01073g contributor: fullname: Qiu, GYS – volume: 82 start-page: 3622 year: 2017 ident: WOS:000398986000027 article-title: Visible-Light-Promoted C-H Arylation by Merging Palladium Catalysis with Organic Photoredox Catalysis publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.7b00140 contributor: fullname: Jiang, J – volume: 52 start-page: 2980 year: 2016 ident: WOS:000369641300026 article-title: Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c5cc09830k contributor: fullname: Zhang, WX – volume: 64 start-page: 10670 year: 2008 ident: WOS:000260844000004 article-title: Hydrothiolation of terminal alkynes with diaryl disulfides and diphenyl diselenide: selective synthesis of (Z)-1-alkenyl sulfides and selenides publication-title: TETRAHEDRON doi: 10.1016/j.tet.2008.09.022 contributor: fullname: Wang, ZL – volume: 13 start-page: 4876 year: 2011 ident: WOS:000294703900032 article-title: DABCO-Bis(sulfur dioxide), DABSO, as a Convenient Source of Sulfur Dioxide for Organic Synthesis: Utility in Sulfonamide and Sulfamide Preparation publication-title: ORGANIC LETTERS doi: 10.1021/ol201957n contributor: fullname: Woolven, H – volume: 4 start-page: 602 year: 2015 ident: WOS:000357386200001 article-title: The Development and Application of Sulfur Dioxide Surrogates in Synthetic Organic Chemistry publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ajoc.201500103 contributor: fullname: Emmett, EJ – volume: 17 start-page: 3170 year: 2015 ident: WOS:000356845000078 article-title: Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2,4,6-Trichlorophenyl Chlorosulfate publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.5b01540 contributor: fullname: Colombe, JR – volume: 12 start-page: 9743 year: 2014 ident: WOS:000345458700002 article-title: Sulfinate derivatives: dual and versatile partners in organic synthesis publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c4ob01727g contributor: fullname: Aziz, J – volume: 4 start-page: 4125 year: 2002 ident: WOS:000179173700035 article-title: Basic and reductive sulfone-directed ring-opening reactions of difluorinated oxa[2.2.1]bicycloheptanes publication-title: ORGANIC LETTERS doi: 10.1021/ol0268743 contributor: fullname: Crowley, PJ – volume: 15 start-page: 2954 year: 2013 ident: WOS:000320979000017 article-title: A Closer Look at the Bromine-Lithium Exchange with tert-Butyllithium in an Aryl Sulfonamide Synthesis publication-title: ORGANIC LETTERS doi: 10.1021/ol4010454 contributor: fullname: Waldmann, C – volume: 16 start-page: 4056 year: 2014 ident: WOS:000339982300053 article-title: A Copper-Catalyzed Three-Component Reaction of Triethoxysilanes, Sulfur Dioxide, and Hydrazines publication-title: ORGANIC LETTERS doi: 10.1021/ol5018849 contributor: fullname: Wang, XB – volume: 287 start-page: 1960 year: 2000 ident: WOS:000085902800046 article-title: Drug discovery: A historical perspective publication-title: SCIENCE contributor: fullname: Drews, J – volume: 42 start-page: 1137 year: 2007 ident: WOS:000249197600011 article-title: Synthesis and antibacterial activity of oxazolidinones containing triazolyl group publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1016/j.ejmech.2007.01.012 contributor: fullname: Fan, H – volume: 11 start-page: 72 year: 2008 ident: WOS:000251872500006 article-title: The sulfonamide group as a structural alert: A distorted story? publication-title: CURRENT OPINION IN DRUG DISCOVERY & DEVELOPMENT contributor: fullname: Smith, DA – year: 1986 ident: 000442118800016.19 publication-title: Synthesis contributor: fullname: Hamada, T. – year: 1983 ident: 000442118800016.3 – volume: 3 start-page: 574 year: 2016 ident: WOS:000374853900007 article-title: Generation of N-aminosulfonamides via a photo-induced fixation of sulfur dioxide into aryl/alkyl halides publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c6qo00060f contributor: fullname: Li, YW – volume: 53 start-page: 6560 year: 2010 ident: WOS:000281753700004 article-title: Synthesis, Anti-Inflammatory Activity, and in Vitro Antitumor Effect of a Novel Class of Cyclooxygenase Inhibitors: 4-(Aryloyl)phenyl Methyl Sulfones publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm100398z contributor: fullname: Harrak, Y – volume: 18 start-page: 508 year: 2016 ident: WOS:000369771800042 article-title: One-Step Synthesis of Sulfonamides from N-Tosylhydrazones publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.5b03545 contributor: fullname: Tsai, AS – volume: 13 start-page: 1592 year: 2015 ident: WOS:000349032400001 article-title: Fixation of sulfur dioxide into small molecules publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c4ob02139h contributor: fullname: Liu, G – volume: 48 start-page: 547 year: 2005 ident: WOS:000226591700024 article-title: Sulfonamide drugs binding to the colchicine site of tubulin: Thermodynamic analysis of the drug-tubulin interactions by isothermal titration calorimetry publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm0494974 contributor: fullname: Banerjee, M – volume: 47 start-page: 2365 year: 2004 ident: 000442118800016.15 publication-title: J. Med. Chem contributor: fullname: Dominique, G. – volume: 53 start-page: 2451 year: 2014 ident: WOS:000336834000018 article-title: Metal-Free Aminosulfonylation of Aryldiazonium Tetrafluoroborates with DABCO center dot(SO2)(2) and Hydrazines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201309851 contributor: fullname: Zheng, DQ – volume: 4 start-page: 1121 year: 2017 ident: WOS:000405862600032 article-title: Generation of benzosultams via a radical process with the insertion of sulfur dioxide publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c7qo00127d contributor: fullname: Zhou, KD – year: 1000 ident: 000442118800016.7 article-title: Top 200 Drugs of 2011 publication-title: Pharmacy Times contributor: fullname: Bartholow, M. – volume: 50 start-page: 8886 year: 2014 ident: WOS:000339861700016 article-title: Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c4cc03032j contributor: fullname: Zheng, DQ – year: 2004 ident: 000442118800016.2 – volume: 50 start-page: 11746 year: 2014 ident: WOS:000342069600031 article-title: Synthesis of 1-(2,3-dihydrobenzofuran-3-yl)-methanesulfonohydrazides through insertion of sulfur dioxide publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c4cc05401f contributor: fullname: An, YY – volume: 48 start-page: 10037 year: 2012 ident: WOS:000308653800026 article-title: A palladium-catalyzed reaction of aryl halides, potassium metabisulfite, and hydrazines publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc34957d contributor: fullname: Ye, SQ – volume: 18 start-page: 524 year: 2016 ident: WOS:000369771800046 article-title: Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.5b03552 contributor: fullname: Wang, M – volume: 48 start-page: 1939 year: 2016 ident: WOS:000380250800005 article-title: Recent Advances in the Synthesis of Sulfones publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-0035-1560444 contributor: fullname: Liu, NW – volume: 20 start-page: 1167 year: 2018 ident: WOS:000426013600068 article-title: Synthesis of Aromatic Sulfonamides through a Copper-Catalyzed Coupling of Aryldiazonium Tetrafluoroborates, DABCO center dot(SO2)(2), and N-Chloroamines publication-title: ORGANIC LETTERS doi: 10.1021/acs.orglett.8b00093 contributor: fullname: Zhang, F – volume: 132 start-page: 16372 year: 2010 ident: WOS:000284792000025 article-title: Palladium-Catalyzed Aminosulfonylation of Aryl Halides publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja1081124 contributor: fullname: Nguyen, B – volume: 48 start-page: 7753 year: 2012 ident: WOS:000306176300029 article-title: A palladium-catalyzed three-component coupling of arylboronic acids, sulfur dioxide and hydrazines publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc33725h contributor: fullname: Ye, SQ – volume: 359 start-page: 2653 year: 2017 ident: WOS:000407065400018 article-title: A Route to O-Aminosulfonates and Sulfonamides through Insertion of Sulfur Dioxide and Hydrogen Atom Transfer publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201700501 contributor: fullname: Liu, T – volume: 47 start-page: 2365 year: 2004 ident: C8CC03778G-(cit3c)/*[position()=1] publication-title: J. Med. Chem. doi: 10.1021/jm031117b contributor: fullname: Dominique – volume: 48 start-page: 547 year: 2005 ident: C8CC03778G-(cit3d)/*[position()=1] publication-title: J. Med. Chem. doi: 10.1021/jm0494974 contributor: fullname: Banerjee – volume: 3 start-page: 574 year: 2016 ident: C8CC03778G-(cit7a)/*[position()=1] publication-title: Org. Chem. Front. doi: 10.1039/C6QO00060F contributor: fullname: Li – volume: 64 start-page: 10670 year: 2008 ident: C8CC03778G-(cit13)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2008.09.022 contributor: fullname: Wang – volume: 11 start-page: 5393 year: 2013 ident: C8CC03778G-(cit5a)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/c3ob40997j contributor: fullname: Bisseret – volume: 50 start-page: 11746 year: 2014 ident: C8CC03778G-(cit6l)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C4CC05401F contributor: fullname: An – volume: 13 start-page: 1592 year: 2015 ident: C8CC03778G-(cit5b)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C4OB02139H contributor: fullname: Liu – volume: 18 start-page: 5848 year: 2016 ident: C8CC03778G-(cit10a)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.6b02894 contributor: fullname: Shavnya – volume: 23 start-page: 203 year: 2013 ident: C8CC03778G-(cit3f)/*[position()=1] publication-title: Expert Opin. Ther. Pat. doi: 10.1517/13543776.2013.742065 contributor: fullname: Scozzafava – volume: 15 start-page: 2954 year: 2013 ident: C8CC03778G-(cit6k)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol4010454 contributor: fullname: Waldmann – volume: 4 start-page: 4125 year: 2002 ident: C8CC03778G-(cit1c)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol0268743 contributor: fullname: Crowley – volume: 4 start-page: 1121 year: 2017 ident: C8CC03778G-(cit6c)/*[position()=1] publication-title: Org. Chem. Front. doi: 10.1039/C7QO00127D contributor: fullname: Zhou – volume: 359 start-page: 2653 year: 2017 ident: C8CC03778G-(cit12b)/*[position()=1] publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.201700501 contributor: fullname: Liu – volume: 12 start-page: 9743 year: 2014 ident: C8CC03778G-(cit1f)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C4OB01727G contributor: fullname: Aziz – volume: 132 start-page: 16372 year: 2010 ident: C8CC03778G-(cit6a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja1081124 contributor: fullname: Nguyen – start-page: 852 year: 1986 ident: C8CC03778G-(cit4)/*[position()=1] publication-title: Synthesis doi: 10.1055/s-1986-31803 contributor: fullname: Hamada – volume: 13 start-page: 4876 year: 2011 ident: C8CC03778G-(cit6e)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol201957n contributor: fullname: Woolven – volume: 18 start-page: 524 year: 2016 ident: C8CC03778G-(cit11)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.5b03552 contributor: fullname: Wang – volume: 135 start-page: 10638 year: 2013 ident: C8CC03778G-(cit6g)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja405949a contributor: fullname: DeBergh – volume: 6 start-page: 198 year: 2004 ident: C8CC03778G-(cit8a)/*[position()=1] publication-title: Green Chem. doi: 10.1039/B315580C contributor: fullname: Ouchi – volume: 53 start-page: 6560 year: 2010 ident: C8CC03778G-(cit3e)/*[position()=1] publication-title: J. Med. Chem. doi: 10.1021/jm100398z contributor: fullname: Harrak – volume: 60 start-page: 1036 year: 2012 ident: C8CC03778G-(cit1g)/*[position()=1] publication-title: J. Agric. Food Chem. doi: 10.1021/jf203772d contributor: fullname: Xu – volume: 4 start-page: 602 year: 2015 ident: C8CC03778G-(cit5c)/*[position()=1] publication-title: Asian J. Org. Chem. doi: 10.1002/ajoc.201500103 contributor: fullname: Emmett – volume: 48 start-page: 10037 year: 2012 ident: C8CC03778G-(cit7d)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/c2cc34957d contributor: fullname: Ye – volume: 55 start-page: 747 year: 2016 ident: C8CC03778G-(cit6f)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201508370 contributor: fullname: Deeming – volume: 37 start-page: 206 year: 1921 ident: C8CC03778G-(cit8c)/*[position()=1] publication-title: J. Soc. Dyers Colour. contributor: fullname: Chappell – volume: 53 start-page: 2451 year: 2014 ident: C8CC03778G-(cit6b)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201309851 contributor: fullname: Zheng – volume: 42 start-page: 1137 year: 2007 ident: C8CC03778G-(cit3b)/*[position()=1] publication-title: Eur. J. Med. Chem. doi: 10.1016/j.ejmech.2007.01.012 contributor: fullname: Fan – volume: 112 start-page: 1650 year: 2012 ident: C8CC03778G-(cit9)/*[position()=2] publication-title: Chem. Rev. doi: 10.1021/cr100175t contributor: fullname: Kotha – volume: 50 start-page: 8886 year: 2014 ident: C8CC03778G-(cit6m)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C4CC03032J contributor: fullname: Zheng – volume: 82 start-page: 3622 year: 2017 ident: C8CC03778G-(cit12a)/*[position()=1] publication-title: J. Org. Chem. doi: 10.1021/acs.joc.7b00140 contributor: fullname: Jiang – volume: 16 start-page: 4056 year: 2014 ident: C8CC03778G-(cit7c)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/ol5018849 contributor: fullname: Wang – volume: 53 start-page: 6560 year: 2010 ident: C8CC03778G-(cit1a)/*[position()=1] publication-title: J. Med. Chem. doi: 10.1021/jm100398z contributor: fullname: Harrak – volume: 48 start-page: 7753 year: 2012 ident: C8CC03778G-(cit7b)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/c2cc33725h contributor: fullname: Ye – volume: 54 start-page: 1168 year: 2015 ident: C8CC03778G-(cit6j)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201409283 contributor: fullname: Deeming – volume: 5 start-page: 691 year: 2018 ident: C8CC03778G-(cit5e)/*[position()=1] publication-title: Org. Chem. Front. doi: 10.1039/C7QO01073G contributor: fullname: Qiu – volume-title: Sulfur Dioxide Insertion Reactions for Organic Synthesis year: 2017 ident: C8CC03778G-(cit5d)/*[position()=1] doi: 10.1007/978-981-10-4202-7 contributor: fullname: Zheng – volume: 287 start-page: 1960 year: 2000 ident: C8CC03778G-(cit2a)/*[position()=1] publication-title: Science doi: 10.1126/science.287.5460.1960 contributor: fullname: Drews – volume: 18 start-page: 508 year: 2016 ident: C8CC03778G-(cit6h)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.5b03545 contributor: fullname: Tsai – volume: 3 start-page: 245 year: 2012 ident: C8CC03778G-(cit1d)/*[position()=1] publication-title: Front. Plant Sci. doi: 10.3389/fpls.2012.00245 contributor: fullname: Noutoshi – volume: 17 start-page: 3170 year: 2015 ident: C8CC03778G-(cit6i)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.5b01540 contributor: fullname: Colombe – volume: 23 start-page: 1421 year: 2015 ident: C8CC03778G-(cit3a)/*[position()=1] publication-title: Bioorg. Med. Chem. doi: 10.1016/j.bmc.2015.02.026 contributor: fullname: Mariusz – start-page: 1939 year: 2016 ident: C8CC03778G-(cit1e)/*[position()=1] publication-title: Synthesis contributor: fullname: Liu – ident: C8CC03778G-(cit2b)/*[position()=1] contributor: fullname: Bartholow – volume: 11 start-page: 72 year: 2008 ident: C8CC03778G-(cit3g)/*[position()=1] publication-title: Curr. Opin. Drug Discovery Dev. contributor: fullname: Smith – volume: 20 start-page: 1167 year: 2018 ident: C8CC03778G-(cit6d)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.8b00093 contributor: fullname: Zhang – volume-title: Pharmaceutical Substances: Syntheses, Patents, Applications year: 1999 ident: C8CC03778G-(cit1h)/*[position()=1] contributor: fullname: Kleeman – volume: 52 start-page: 2980 year: 2016 ident: C8CC03778G-(cit10b)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C5CC09830K contributor: fullname: Zhang – volume: 11 start-page: 72 year: 2008 ident: C8CC03778G-(cit1b)/*[position()=1] publication-title: Curr. Opin. Drug Discovery Dev. contributor: fullname: Smith |
| SSID | ssj0000158 |
| Score | 2.4936218 |
| Snippet | A simple and convenient method for N-aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free,... A simple and convenient method for N -aminosulfonamide synthesis from the cross-coupling of aryldiazonium tetrafluoroborates and rongalite under metal-free,... |
| Source | Web of Science |
| SourceID | proquest crossref pubmed webofscience |
| SourceType | Aggregation Database Index Database Enrichment Source |
| StartPage | 7641 |
| SubjectTerms | Aromatic compounds Chemical reduction Chemical synthesis Chemistry Chemistry, Multidisciplinary Coupling Cross coupling Physical Sciences Reagents Science & Technology Sulfur dioxide |
| Title | The triple role of rongalite in aminosulfonylation of aryldiazonium tetrafluoroborates: synthesis of N-aminosulfonamides via a radical coupling reaction |
| URI | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000442118800016 https://www.ncbi.nlm.nih.gov/pubmed/29931018 https://www.proquest.com/docview/2064199531 https://search.proquest.com/docview/2058504503 |
| Volume | 54 |
| WOS | 000442118800016 |
| WOSCitedRecordID | wos000442118800016 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV07b9swECYSZ2iWou-4TQsWzWYolUxRj26pkCYNmix1UG8GRVGBAVsyZKlA8kv6c3ukSJmOPbhdBJmiaVr36Xh3uvuI0ElIaUajOHVcX0SO72XUSTk4KyzgYH2LOBymslD4-ia4vPWvxnS8t39oZS01dXrKH7bWlfyPVKEN5CqrZP9Bst2g0ADnIF84goThuLOM60rlA5oswaos7qRprbhA2HxalMtmlsv08842ZNX9DFDxAE9zMx_Uoq5YPmvKqlRwaHPklvcFWIaarOTGsQaC00wsB79lMdegYplmGGkWqq4dTFDeidoQIBhOAm4Xo6hob1cxplRyu5-IFZv4pYPZ11NWrkIMbdvX0oGB9bpr9b1qCueCrdrHU3NhytQ37DiHVsptapSMo_ws-SAxe-BZCpvQ2AlJS0l5KnRb4DvgiY1tLd9SVWs0U2rp7DBoqbf0-g8f_a1ri0skNSuPOHdJGEZ3dieQzGKuUAbLO_HM9NfovR8tu10ypHqpDn44aFJpgO-jgyEoTdpDB2fno-8_LDI0tdts948N2S6JP68mJcmt9QzWLa0N92mrpaWsqtEz9FS7Q_isxfZztCeKF-hJJ4GX6A9gHLcYxxLjuMxxh3E8LfAmxmWXNYzjTYx_wR3CZfctCMeAcMywRjg2CMcG4a_Q7bfzUXLp6N1EHE48WjtxLOJIuHlK_TCnvvBI7osgFLkI4mEa5C53gzgH7yBXToMbchYxAt70MJP15Cl5jXpFWYgjhEkIZnCe-oIy7hPmpUFGUzA2GZjTaRR6ffTJ3PnJoiWNmahkDxJPkihJlKgu-ujYCGWilcpyMgQXQbImEBjkY3cZ7rl8j8cKUTayD8wKXDGX9NGbVpjdzxjh99GJLd3u-iOw9ZG3S7dE7xcgeTLqt7sN_Q4dyse4DVceo15dNeI9GPB1-kEj-y8lXPTu |
| link.rule.ids | 315,783,787,4031,27935,27936,27937 |
| 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=The+triple+role+of+rongalite+in+aminosulfonylation+of+aryldiazonium+tetrafluoroborates%3A+synthesis+of+N-aminosulfonamides+via+a+radical+coupling+reaction&rft.jtitle=Chemical+communications+%28Cambridge%2C+England%29&rft.au=Wang%2C+Miao&rft.au=Tang%2C+Bo-Cheng&rft.au=Wang%2C+Jun-Gang&rft.au=Xiang%2C+Jia-Chen&rft.date=2018&rft.pub=Royal+Soc+Chemistry&rft.issn=1359-7345&rft.eissn=1364-548X&rft.volume=54&rft.issue=55&rft.spage=7641&rft.epage=7644&rft_id=info:doi/10.1039%2Fc8cc03778g&rft_id=info%3Apmid%2F29931018&rft.externalDBID=n%2Fa&rft.externalDocID=000442118800016 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1359-7345&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1359-7345&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1359-7345&client=summon |