Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Minh Loan Tran Do"'
Publikováno v:
ACS Applied Polymer Materials. 4:1401-1410
Publikováno v:
Polymer Chemistry
Polymer Chemistry, Royal Society of Chemistry-RSC, 2021, 12 (31), pp.4508-4523. ⟨10.1039/d1py00685a⟩
Polymer Chemistry, Royal Society of Chemistry-RSC, 2021, 12 (31), pp.4508-4523. ⟨10.1039/d1py00685a⟩
2-Trifluoromethacrylic acid (MAF) is a peculiar fluorinated functional monomer. Though it is known to polymerise via CC bond cleavage under anionic initiation, its oxa-Michael addition polymerisation afforded polyesters bearing trifluoromethyl side g
Autor:
Gabin Mwande-Maguene, Hooriye Boosaliki, Jean-Luc Pirat, Minh Loan Tran Do, Jacques Lebibi, David Virieux, Tahar Ayad, Mina Hariri, Nora Sechet, Karen-Pacelye Mengue Me Ndong, Geraud Chacktas, Fatemeh Darvish, A. R. Burilov
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2021, 86 (11), pp.7813-7824. ⟨10.1021/acs.joc.1c00648⟩
Journal of Organic Chemistry, American Chemical Society, 2021, 86 (11), pp.7813-7824. ⟨10.1021/acs.joc.1c00648⟩
Gold(I)-catalyzed reactions of electron-poor alkynes are still a challenging process. A straightforward synthesis of phosphorus-based heterocycles, namely, 2-phenyl 1H-isophosphinoline 2-oxides 1, is reported. The reaction used PPh3AuCl precatalyst i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc24bdcfccff324fa773dd4f230281e9
https://hal.umontpellier.fr/hal-03284163
https://hal.umontpellier.fr/hal-03284163
Publikováno v:
Coord. Chem. Rev.
Coord. Chem. Rev., 2015, 288, pp.50-68. ⟨10.1016/j.ccr.2015.01.008⟩
Coord. Chem. Rev., 2015, 288, pp.50-68. ⟨10.1016/j.ccr.2015.01.008⟩
This review presents recent advances in reduction of carboxylic and carbonic derivatives by means of iron catalysis. It reveals the strong efforts, which have been devoted to the discovery of new ligands and catalysts during the last decade.
Autor:
Cyril Lebargy, Minh-Loan Tran Do, Clothilde Le Guen, Aurélien Chardon, Thierry Lequeux, Jean-François Lohier, Emmanuel Pfund
Publikováno v:
ChemInform. 47
Study of the intramolecular aza-Michael addition reaction from an aminofluorovinylsulfone opens a new route for the synthesis of pyrrolidine derivatives. An unexpected diastereoselective cyclization reaction was observed, leading preferentially to th
Autor:
Minh-Loan Tran Do, Cyril Lebargy, Thierry Lequeux, Aurélien Chardon, Clothilde Le Guen, Jean-François Lohier, Emmanuel Pfund
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (15), pp.6714-6720. ⟨10.1021/acs.joc.6b01363⟩
Congrès carbanion Chem ISCC
Congrès carbanion Chem ISCC, Jul 2016, rouen, France
CFCF
CFCF, May 2017, Murol, France
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (15), pp.6714-6720. ⟨10.1021/acs.joc.6b01363⟩
Congrès carbanion Chem ISCC
Congrès carbanion Chem ISCC, Jul 2016, rouen, France
CFCF
CFCF, May 2017, Murol, France
Study of the intramolecular aza-Michael addition reaction from an aminofluorovinylsulfone opens a new route for the synthesis of pyrrolidine derivatives. An unexpected diastereoselective cyclization reaction was observed, leading preferentially to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6018bf56dddfa5a4821f4f2597641da0
https://hal.archives-ouvertes.fr/hal-01829969
https://hal.archives-ouvertes.fr/hal-01829969
Publikováno v:
Angewandte Chemie. 126:13218-13220
Publikováno v:
ChemInform. 46
This review presents recent advances in reduction of carboxylic and carbonic derivatives by means of iron catalysis. It reveals the strong efforts, which have been devoted to the discovery of new ligands and catalysts during the last decade.
Publikováno v:
ChemInform. 46
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2014, 53 (48), pp.13004-13006. ⟨10.1002/anie.20140761310.1002/ange.201407613⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2014, 53 (48), pp.13004-13006. ⟨10.1002/anie.20140761310.1002/ange.201407613⟩
International audience