Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Claire Chatalova-Sazepin"'
Xenon Difluoride Mediated Fluorodecarboxylations for the Syntheses of Di- and Trifluoromethoxyarenes
Autor:
Benjamin R. Boswell, Claire Chatalova-Sazepin, Maxim Epifanov, Glenn M. Sammis, Meruyert Binayeva, Manu Jagdeo, Carolyn Amador, Paul J. Foth, Wei Zhang
Publikováno v:
Organic Letters. 18:4570-4573
XeF2 is demonstrated to be a more proficient fluorine-transfer reagent than either NFSI or Selectfluor in fluorodecarboxylations of both mono- and difluoroaryloxy acetic acid derivatives. This method efficiently converts a wide range of neutral and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08dc2114c434605ec0f69ea84328159
https://doi.org/10.1021/acs.orglett.6b02208
https://doi.org/10.1021/acs.orglett.6b02208
Publikováno v:
Synthesis. 47:2554-2569
The importance of fluorinated compounds in pharmaceutical, agrochemical, and material chemistry has led to the development of numerous methods for electrophilic and nucleophilic fluorination. Radical fluorination represents an interesting complementa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd7e3d8a4d3ea4d7748d64cc150ee2a
https://doi.org/10.1055/s-0034-1378824
https://doi.org/10.1055/s-0034-1378824
Publikováno v:
Angewandte Chemie. 127:5533-5536
A three-component carboetherification of unactivated alkenes has been developed allowing the rapid building of complexity from simple starting materials. A wide range of α-substituted styrenes underwent smooth reactions with unactivated alkyl nitril
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6988cfce7806ebd47b68d8b4dc363ef3
https://doi.org/10.1002/ange.201412357
https://doi.org/10.1002/ange.201412357
Publikováno v:
ChemInform. 47
A copper-catalyzed three-component reaction of alkenes, alkylnitriles, and water affords γ-butyrolactones in good yields. The domino process involves an unprecedented hydroxy-cyanoalkylation of alkenes and subsequent lactonization with the creation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::052477249a410e97cb429e2c3514f5a5
https://doi.org/10.1002/chin.201649110
https://doi.org/10.1002/chin.201649110
Publikováno v:
Angewandte Chemie (International ed. in English). 55(32)
A copper-catalyzed three-component reaction of alkenes, alkylnitriles, and water affords γ-butyrolactones in good yields. The domino process involves an unprecedented hydroxy-cyanoalkylation of alkenes and subsequent lactonization with the creation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b50606350c676917c392f29e58608011
https://pubmed.ncbi.nlm.nih.gov/27337057
https://pubmed.ncbi.nlm.nih.gov/27337057
Autor:
Pierre Kennepohl, Joe C. T. Leung, Jean-François Paquin, Glenn M. Sammis, Tulin Okbinoglu, Claire Chatalova Sazepin, Montserrat Rueda-Becerril
Publikováno v:
Journal of the American Chemical Society. 134:4026-4029
The development of new synthetic technologies for the selective fluorination of organic compounds has increased with the escalating importance of fluorine-containing pharmaceuticals. Traditional methods potentially applicable to drug synthesis rely o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee917e01690bc9fff9ceeb4dce1cfa31
https://doi.org/10.1021/ja211679v
https://doi.org/10.1021/ja211679v
Publikováno v:
ChemInform. 46
The importance of fluorinated compounds in pharmaceutical, agrochemical, and material chemistry has led to the development of numerous methods for electrophilic and nucleophilic fluorination. Radical fluorination represents an interesting complementa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7a9e7474104f43bed7dd5a5224f2d83
https://doi.org/10.1002/chin.201544259
https://doi.org/10.1002/chin.201544259
Publikováno v:
ChemInform. 46
A three-component carboetherification of unactivated alkenes has been developed allowing the rapid building of complexity from simple starting materials. A wide range of α-substituted styrenes underwent smooth reactions with unactivated alkyl nitril
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8365f87f2951d4dedd2a9731a3333bd
https://doi.org/10.1002/chin.201536062
https://doi.org/10.1002/chin.201536062
Autor:
Montserrat Rueda-Becerril, Joe C. T. Leung, Jean-François Paquin, Claire Chatalova-Sazepin, Glenn M. Sammis, Julian G. West
Publikováno v:
ChemInform. 44
Photolysis of the title compounds in the presence of Selectfluor results in decarboxylative fluorination to afford fluoromethyl ethers and benzyl fluorides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a104277868c878f081d49e6dc8ad3a40
https://doi.org/10.1002/chin.201312050
https://doi.org/10.1002/chin.201312050
Autor:
Jean-François Paquin, Julian G. West, Joe C. T. Leung, Claire Chatalova-Sazepin, Glenn M. Sammis, Montserrat Rueda-Becerril
Publikováno v:
Angewandte Chemie (International ed. in English). 51(43)
Photolysis of the title compounds in the presence of Selectfluor results in decarboxylative fluorination to afford fluoromethyl ethers and benzyl fluorides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27928ac11564eedd602b4b63e4d61201
https://pubmed.ncbi.nlm.nih.gov/23023887
https://pubmed.ncbi.nlm.nih.gov/23023887