Year |
Citation |
Score |
2024 |
Leone M, Milton J, Gryko D, Neuville L, Masson G. TBADT-Mediated Photocatalytic Stereoselective Radical Alkylation of Chiral N-Sulfinyl Imines: Towards Efficient Synthesis of Diverse Chiral Amines. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400363. PMID 38376252 DOI: 10.1002/chem.202400363 |
0.438 |
|
2023 |
Serafino A, Pierre H, Le Vaillant F, Boutet J, Guillamot G, Neuville L, Masson G. Visible-Light-Driven Decarboxylative Borylation: Rapid Access to α- and β-Amino-boronamides. Organic Letters. PMID 38113295 DOI: 10.1021/acs.orglett.3c04067 |
0.35 |
|
2023 |
Di Terlizzi L, Nicchio L, Callegari C, Scaringi S, Neuville L, Fagnoni M, Protti S, Masson G. Visible-Light-Mediated Divergent and Regioselective Vicinal Difunctionalization of Styrenes with Arylazo Sulfones. Organic Letters. 25: 9047-9052. PMID 38085821 DOI: 10.1021/acs.orglett.3c03786 |
0.415 |
|
2023 |
Naulin E, Lombard M, Gandon V, Retailleau P, Elslande EV, Neuville L, Masson G. Enantioselective and Regiodivergent Synthesis of Dihydro-1,2-oxazines from Triene-Carbamates via Chiral Phosphoric Acid-Catalysis. Journal of the American Chemical Society. PMID 38011838 DOI: 10.1021/jacs.3c12015 |
0.473 |
|
2023 |
Bouchet D, Van Elslande E, Masson G. Isothiourea-Catalyzed Enantioselective Synthesis of -3,4-Dihydrothiopyranones: Harnessing Thiochalcones as Original Michael Acceptors. Organic Letters. PMID 37430385 DOI: 10.1021/acs.orglett.3c02011 |
0.471 |
|
2022 |
Lyu J, Claraz A, Retailleau P, Masson G. Divergent cyclodimerizations of styrylnaphthols under aerobic visible-light irradiation and Brønsted acid catalysis. Organic & Biomolecular Chemistry. 20: 9593-9599. PMID 36412533 DOI: 10.1039/d2ob01509a |
0.462 |
|
2022 |
Bouchet D, Varlet T, Masson G. Strategies toward the Difunctionalizations of Enamide Derivatives for Synthesizing α,β-Substituted Amines. Accounts of Chemical Research. 55: 3265-3283. PMID 36318762 DOI: 10.1021/acs.accounts.2c00540 |
0.35 |
|
2022 |
Saidah M, Mardjan MID, Masson G, Parrain JL, Commeiras L. Enantioselective Construction of Tetrasubstituted Carbon Stereocenters via Chiral Phosphoric Acid-Catalyzed Friedel-Craft Alkylation of Indoles with 5-Substituted Hydroxybutyrolactams. Organic Letters. 24: 5298-5303. PMID 35834747 DOI: 10.1021/acs.orglett.2c01898 |
0.368 |
|
2022 |
Varlet T, Bouchet D, Van Elslande E, Masson G. Decatungstate-Photocatalyzed Dearomative Hydroacylation of Indoles: Direct Synthesis of 2-Acylindolines. Chemistry (Weinheim An Der Bergstrasse, Germany). e202201707. PMID 35809229 DOI: 10.1002/chem.202201707 |
0.477 |
|
2021 |
Lyu J, Leone M, Claraz A, Allain C, Neuville L, Masson G. Syntheses of new chiral chimeric photo-organocatalysts. Rsc Advances. 11: 36663-36669. PMID 35494356 DOI: 10.1039/d1ra06885g |
0.309 |
|
2021 |
Claraz A, Allain C, Masson G. Electroreductive Cross-Coupling of Trifluoromethyl Alkenes and Redox Active Esters for the Synthesis of Gem-Difluoroalkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34761845 DOI: 10.1002/chem.202103337 |
0.382 |
|
2021 |
Varlet T, Matišić M, Van Elslande E, Neuville L, Gandon V, Masson G. Enantioselective and Diastereodivergent Synthesis of Spiroindolenines via Chiral Phosphoric Acid-Catalyzed Cycloaddition. Journal of the American Chemical Society. 143: 11611-11619. PMID 34296854 DOI: 10.1021/jacs.1c04648 |
0.477 |
|
2021 |
Varlet T, Masson G. Enamides and dienamides in phosphoric acid-catalysed enantioselective cycloadditions for the synthesis of chiral amines. Chemical Communications (Cambridge, England). 57: 4089-4105. PMID 33908458 DOI: 10.1039/d1cc00590a |
0.426 |
|
2021 |
Ma WY, Gelis C, Bouchet D, Retailleau P, Moreau X, Neuville L, Masson G. Chiral Phosphoric Acid-Catalyzed Enantioselective Construction of 2,3-Disubstituted Indolines. Organic Letters. 23: 442-448. PMID 33404248 DOI: 10.1021/acs.orglett.0c03947 |
0.433 |
|
2021 |
Claraz A, Djian A, Masson G. Electrochemical tandem trifluoromethylation of allylamines/formal (3 + 2)-cycloaddition for the rapid access to CF3-containing imidazolines and oxazolidines Organic Chemistry Frontiers. 8: 288-296. DOI: 10.1039/d0qo01307b |
0.371 |
|
2020 |
Lyu J, Claraz A, Vitale MR, Allain C, Masson G. Preparation of Chiral Photosensitive Organocatalysts and their Application for the Enantioselective Synthesis of 1,2-diamines. The Journal of Organic Chemistry. PMID 32957790 DOI: 10.1021/Acs.Joc.0C01931 |
0.399 |
|
2020 |
Courant T, Lombard M, Boyarskaya DV, Neuville L, Masson G. Tritylium assisted iodine catalysis for the synthesis of unsymmetrical triarylmethanes. Organic & Biomolecular Chemistry. PMID 32789393 DOI: 10.1039/d0ob01502d |
0.399 |
|
2020 |
Le T, Galmiche L, Masson G, Allain C, Audebert P. A straightforward synthesis of a new family of molecules: 2,5,8-trialkoxyheptazines. Application to photoredox catalyzed transformations. Chemical Communications (Cambridge, England). PMID 32789351 DOI: 10.1039/d0cc05118g |
0.342 |
|
2020 |
Varlet T, Gelis C, Retailleau P, Bernadat G, Neuville L, Masson G. Redox-Divergent Chiral Phosphoric Acid-Catalyzed Enantioselective Formal Quinone Diels-Alder Reactions. Angewandte Chemie (International Ed. in English). PMID 32112662 DOI: 10.1002/Anie.202000838 |
0.505 |
|
2020 |
Claraz A, Courant T, Masson G. Electrochemical Intramolecular Oxytrifluoromethylation of -Tethered Alkenyl Alcohols: Synthesis of Functionalized Morpholines. Organic Letters. PMID 32017576 DOI: 10.1021/acs.orglett.0c00176 |
0.314 |
|
2020 |
Varlet T, Neuville L, Masson G. Selective Double C–H Functionalization: A 4-Component Catellani Reaction Chem. 6: 1855-1858. DOI: 10.1016/j.chempr.2020.07.020 |
0.309 |
|
2020 |
Varlet T, Gelis C, Retailleau P, Bernadat G, Neuville L, Masson G. Redox‐Divergent Chiral Phosphoric Acid‐Catalyzed Enantioselective Formal Quinone Diels–Alder Reactions Angewandte Chemie. DOI: 10.1002/Ange.202000838 |
0.482 |
|
2019 |
Gandon V, Jarrige LJ, Masson G. Enantioselective synthesis of complex fused heterocycles via chiral phosphoric-acid catalyzed intramolecular inverse-electron demand aza-Diels-Alder reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31663177 DOI: 10.1002/Chem.201904902 |
0.513 |
|
2019 |
Levitre G, Dagousset G, Anselmi E, Tuccio B, Magnier E, Masson G. Four-Component Photoredox-Mediated Azidoalkoxy-trifluoromethylation of Alkenes. Organic Letters. PMID 31339319 DOI: 10.1021/acs.orglett.9b02152 |
0.739 |
|
2019 |
Jarrige L, Glavač D, Levitre G, Retailleau P, Bernadat G, Neuville L, Masson G. Chiral phosphoric acid-catalyzed enantioselective construction of structurally diverse benzothiazolopyrimidines. Chemical Science. 10: 3765-3769. PMID 31015920 DOI: 10.1039/C8Sc05581E |
0.742 |
|
2019 |
Varlet T, Levitre G, Retailleau P, Masson G. Catalyst-free cycloaddition of 1,3-diene-1-carbamates with azodicarboxylates: A rapid click reaction. Bioorganic & Medicinal Chemistry. PMID 30755349 DOI: 10.1016/j.bmc.2019.02.008 |
0.735 |
|
2019 |
Gelis C, Levitre G, Guérineau V, Touboul D, Neuville L, Masson G. Cover Feature: Tandem Chiral Cu(II) Phosphate-Catalyzed Deoxygenation of Nitrones/Enantioselective Povarov Reaction with Enecarbamates (Eur. J. Org. Chem. 31-32/2019) European Journal of Organic Chemistry. 2019: 4971-4971. DOI: 10.1002/EJOC.201901089 |
0.316 |
|
2019 |
Gelis C, Levitre G, Guérineau V, Touboul D, Neuville L, Masson G. Tandem Chiral Cu(II) Phosphate-Catalyzed Deoxygenation of Nitrones/Enantioselective Povarov Reaction with Enecarbamates European Journal of Organic Chemistry. 2019: 5151-5155. DOI: 10.1002/EJOC.201900547 |
0.329 |
|
2019 |
Levitre G, Audubert C, Dumoulin A, Goual N, Retailleau P, Moreau X, Masson G. Cover Feature: Combining Organocatalysis and Photoredox Catalysis: An Asymmetric Synthesis of Chiral
β‐
Amino
α‐
Substituted Tryptamines (ChemCatChem 23/2019) Chemcatchem. 11: 5659-5659. DOI: 10.1002/cctc.201902113 |
0.37 |
|
2019 |
Levitre G, Audubert C, Dumoulin A, Goual N, Retailleau P, Moreau X, Masson G. Combining Organocatalysis and Photoredox Catalysis: An Asymmetric Synthesis of Chiral
β‐
Amino
α‐
Substituted Tryptamines Chemcatchem. 11: 5723-5727. DOI: 10.1002/cctc.201901266 |
0.41 |
|
2018 |
Claraz A, Masson G. Asymmetric iodine catalysis-mediated enantioselective oxidative transformations. Organic & Biomolecular Chemistry. PMID 30024581 DOI: 10.1039/c8ob01378k |
0.309 |
|
2018 |
Gelis C, Levitre G, Merad J, Retailleau P, Neuville L, Masson G. Highly Diastereo- and Enantioselective Synthesis of Cyclo-hepta[b]indoles via Chiral Phosphoric Acid-Catalyzed (4+3)-Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 30006960 DOI: 10.1002/Anie.201807069 |
0.756 |
|
2018 |
Bortoluzzi J, Jha V, Levitre G, Fer MJ, Berreur J, Masson G, Panossian A, Leroux FR. A stereoselectivity switch in the trapping of polar organometallics with Andersen's reagent - Access to highly stereoenriched transformable biphenyls. The Journal of Organic Chemistry. PMID 29799196 DOI: 10.1021/Acs.Joc.8B00648 |
0.718 |
|
2017 |
Merad J, Lalli C, Bernadat G, Maury J, Masson G. Enantioselective Brønsted Acid Catalysis as a Tool for the Synthesis of Natural Products and Pharmaceuticals. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28981209 DOI: 10.1002/Chem.201703556 |
0.405 |
|
2017 |
Levitre G, Dumoulin A, Retailleau P, Panossian A, Leroux FR, Masson G. Asymmetric α-Sulfonyl- and α-Phosphoryl-oxylation of Ketones by a Chiral Hypervalent Iodine(III). The Journal of Organic Chemistry. PMID 28731345 DOI: 10.1021/Acs.Joc.7B01597 |
0.717 |
|
2017 |
Masson G, Jarrige L, Blanchard F. Enantioselective Organocatalytic Intramolecular aza-Diels-Alder Reaction. Angewandte Chemie (International Ed. in English). PMID 28661020 DOI: 10.1002/anie.201705746 |
0.479 |
|
2017 |
Dumoulin A, Bernadat G, Masson G. Enantioselective three-component amination of enecarbamates enables the synthesis of structurally complex small molecules. The Journal of Organic Chemistry. PMID 28092703 DOI: 10.1021/Acs.Joc.6B03093 |
0.477 |
|
2017 |
Jarrige L, Merad J, Zaied S, Blanchard F, Masson G. Easy Access to Quinolin-2(1H)-ones via a One-Pot Tandem Oxa-Michael–Aldol Sequence Synlett. 28: 1724-1728. DOI: 10.1055/S-0036-1588470 |
0.356 |
|
2016 |
Gelis C, Dumoulin A, Bekkaye M, Neuville L, Masson G. Chiral Hypervalent Iodine(III) Catalyst Promotes Highly Enantioselective Sulfonyl- and Phosphoryl-oxylactonizations. Organic Letters. PMID 28009522 DOI: 10.1021/acs.orglett.6b03631 |
0.49 |
|
2016 |
Gelis C, Bekkaye M, Lebée C, Blanchard F, Masson G. Chiral Phosphoric Acid Catalyzed [3 + 2] Cycloaddition and Tandem Oxidative [3 + 2] Cycloaddition: Asymmetric Synthesis of Substituted 3-Aminodihydrobenzofurans. Organic Letters. PMID 27352020 DOI: 10.1021/acs.orglett.6b01593 |
0.453 |
|
2016 |
Dumoulin A, Masson G. Asymmetric Oxidative Nitroso-Diels-Alder Reaction of N-Arylhydroxylamines Catalyzed by a Chiral Phosphoric Acid. The Journal of Organic Chemistry. PMID 27337410 DOI: 10.1021/acs.joc.6b01256 |
0.432 |
|
2016 |
Jarrige L, Levitre G, Masson G. Visible Light Photoredox-Catalyzed Coupling Reaction of Azoles with alpha- Carbamoylsulfides. The Journal of Organic Chemistry. PMID 27314573 DOI: 10.1021/acs.joc.6b01108 |
0.74 |
|
2016 |
Jarrige L, Carboni A, Dagousset G, Levitre G, Magnier E, Masson G. Photoredox-Catalyzed Three-Component Tandem Process: An Assembly of Complex Trifluoromethylated Phthalans and Isoindolines. Organic Letters. PMID 27276522 DOI: 10.1021/acs.orglett.6b01257 |
0.712 |
|
2016 |
Lebée C, Languet M, Allain C, Masson G. α-Carbamoylsulfides as N-Carbamoylimine Precursors in the Visible Light Photoredox-Catalyzed Synthesis of α,α-Disubstituted Amines. Organic Letters. 18: 1478-81. PMID 26950249 DOI: 10.1021/Acs.Orglett.6B00442 |
0.312 |
|
2016 |
Bekkaye M, Masson G. Synthesis of New Axially Chiral Iodoarenes Synthesis (Germany). 48: 302-312. DOI: 10.1055/s-0035-1560512 |
0.328 |
|
2016 |
Jarrige L, Levitre G, Masson G. ChemInform Abstract: Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides. Cheminform. 47. DOI: 10.1002/CHIN.201652260 |
0.349 |
|
2015 |
Pous J, Courant T, Bernadat G, Iorga BI, Blanchard F, Masson G. Regio-, Diastereo-, and Enantioselective Nitroso-Diels-Alder Reaction of 1,3-Diene-1-carbamates Catalyzed by Chiral Phosphoric Acids. Journal of the American Chemical Society. 137: 11950-3. PMID 26355670 DOI: 10.1021/Jacs.5B08515 |
0.499 |
|
2015 |
Lebée C, Kataja AO, Blanchard F, Masson G. Formal Asymmetric Organocatalytic [3+2] Cyclization between Enecarbamates and 3-Indolylmethanols: Rapid Access to 3-Aminocyclopenta[b]indoles. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8399-402. PMID 25892287 DOI: 10.1002/chem.201500749 |
0.458 |
|
2015 |
Dumoulin A, Lalli C, Retailleau P, Masson G. Catalytic, highly enantioselective, direct amination of enecarbamates. Chemical Communications (Cambridge, England). 51: 5383-6. PMID 25426504 DOI: 10.1039/c4cc08052a |
0.376 |
|
2015 |
Lalli C, Dumoulin A, Lebée C, Drouet F, Guérineau V, Touboul D, Gandon V, Zhu J, Masson G. Chiral calcium-BINOL phosphate catalyzed diastereo- and enantioselective synthesis of syn-1,2-disubstituted 1,2-diamines: scope and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1704-12. PMID 25418548 DOI: 10.1002/Chem.201405286 |
0.306 |
|
2015 |
List B, Höfler D, Pous J, Courant T, Bernadat G, Iorga BI, Blanchard F, Masson G. Phosphoric Acid-Catalyzed Asymmetric Nitroso-Diels–Alder Reaction Synfacts. 11: 1212-1212. DOI: 10.1055/S-0035-1560719 |
0.405 |
|
2014 |
Carboni A, Dagousset G, Magnier E, Masson G. One pot and selective intermolecular aryl- and heteroaryl-trifluoromethylation of alkenes by photoredox catalysis. Chemical Communications (Cambridge, England). 50: 14197-200. PMID 25285576 DOI: 10.1039/c4cc07066f |
0.411 |
|
2014 |
Dagousset G, Carboni A, Magnier E, Masson G. Photoredox-induced three-component azido- and aminotrifluoromethylation of alkenes. Organic Letters. 16: 4340-3. PMID 25102254 DOI: 10.1021/ol5021477 |
0.389 |
|
2014 |
Dagousset G, Erb W, Zhu J, Masson G. Phosphoric acid catalyzed diastereo- and enantioselective synthesis of substituted 1,3-diaminotetralins. Organic Letters. 16: 2554-7. PMID 24762190 DOI: 10.1021/Ol500946W |
0.372 |
|
2014 |
George N, Bekkaye M, Alix A, Zhu J, Masson G. NIS-assisted aza-Friedel-Crafts reaction with α-carbamoysulfides as precursors of N-carbamoylimines. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3621-5. PMID 24615749 DOI: 10.1002/Chem.201400117 |
0.331 |
|
2014 |
Bekkaye M, Masson G. Cerium(IV) ammonium nitrate mediated three-component α-allylation of imine surrogates. Organic Letters. 16: 1510-3. PMID 24568134 DOI: 10.1021/ol5004143 |
0.372 |
|
2014 |
Bernadat G, Masson G. Enamide derivatives: Versatile building blocks for highly functionalized α,β-substituted amines Synlett. 25. DOI: 10.1055/S-0034-1379166 |
0.303 |
|
2014 |
Kataja AO, Masson G. Imine and iminium precursors as versatile intermediates in enantioselective organocatalysis Tetrahedron. 70: 8783-8815. DOI: 10.1016/j.tet.2014.06.101 |
0.466 |
|
2014 |
Kataja AO, Masson G. ChemInform Abstract: Imine and Iminium Precursors as Versatile Intermediates in Enantioselective Organocatalysis Cheminform. 46: no-no. DOI: 10.1002/CHIN.201503244 |
0.416 |
|
2014 |
Dagousset G, Erb W, Zhu J, Masson G. ChemInform Abstract: Phosphoric Acid Catalyzed Diastereo- and Enantioselective Synthesis of Substituted 1,3-Diaminotetralins. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201446114 |
0.383 |
|
2014 |
Brioche J, Courant T, Alcaraz L, Stocks M, Furber M, Zhu J, Masson G. ChemInform Abstract: Chiral Phosphoric Acid-Catalyzed Enantioselective Three- Component Aza-Diels-Alder Reactions of Aminopyrroles and Aminopyrazoles. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201445175 |
0.482 |
|
2014 |
Masson G. Catalytic Cascade Reactions. Edited by Peng-Fei Xu and Wei Wang. Angewandte Chemie International Edition. 53: 13656-13657. DOI: 10.1002/ANIE.201409867 |
0.393 |
|
2014 |
Brioche J, Courant T, Alcaraz L, Stocks M, Furber M, Zhu J, Masson G. Chiral phosphoric acid-catalyzed enantioselective three- component aza-diels-alder reactions of aminopyrroles and aminopyrazoles Advanced Synthesis and Catalysis. 356: 1719-1724. DOI: 10.1002/Adsc.201400093 |
0.499 |
|
2013 |
He L, Laurent G, Retailleau P, Folléas B, Brayer JL, Masson G. Highly enantioselective aza-Diels-Alder reaction of 1-azadienes with enecarbamates catalyzed by chiral phosphoric acids. Angewandte Chemie (International Ed. in English). 52: 11088-91. PMID 24038965 DOI: 10.1002/anie.201304969 |
0.47 |
|
2013 |
Drouet F, Masson G, Zhu J. Ugi four-component reaction of alcohols: stoichiometric and catalytic oxidation/MCR sequences. Organic Letters. 15: 2854-7. PMID 23701665 DOI: 10.1021/Ol401181A |
0.333 |
|
2013 |
Masson G, Lalli C, Benohoud M, Dagousset G. Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles. Chemical Society Reviews. 42: 902-23. PMID 23172010 DOI: 10.1039/c2cs35370a |
0.423 |
|
2013 |
Courant T, Kumarn S, He L, Retailleau P, Masson G. ChemInform Abstract: Chiral Phosphoric Acid-Catalyzed Enantioselective Aza-Friedel-Crafts Alkylation of Indoles with γ-Hydroxy-γ-lactams. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201332129 |
0.38 |
|
2013 |
Drouet F, Zhu J, Masson G. Iron chloride-catalyzed three-component domino sequences: Syntheses of functionalized α-Oxy-N-acylhemiaminals and α-Oxyimides Advanced Synthesis and Catalysis. 355: 3563-3569. DOI: 10.1002/Adsc.201300847 |
0.306 |
|
2013 |
Courant T, Kumarn S, He L, Retailleau P, Masson G. Chiral phosphoric acid-catalyzed enantioselective aza-Friedel-Crafts alkylation of indoles with γ-hydroxy-γ-lactams Advanced Synthesis and Catalysis. 355: 836-840. DOI: 10.1002/adsc.201201008 |
0.381 |
|
2012 |
Gualtierotti JB, Schumacher X, Fontaine P, Masson G, Wang Q, Zhu J. Amidation of aldehydes and alcohols through α-iminonitriles and a sequential oxidative three-component Strecker reaction/thio-Michael addition/alumina-promoted hydrolysis process to access β-mercaptoamides from aldehydes, amines, and thiols. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14812-9. PMID 23019046 DOI: 10.1002/Chem.201202291 |
0.342 |
|
2012 |
Su Y, Bouma MJ, Alcaraz L, Stocks M, Furber M, Masson G, Zhu J. Organocatalytic enantioselective one-pot four-component ugi-type multicomponent reaction for the synthesis of epoxy-tetrahydropyrrolo[3,4-b]pyridin-5-ones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12624-7. PMID 22930594 DOI: 10.1002/Chem.201202174 |
0.488 |
|
2012 |
Alix A, Lalli C, Retailleau P, Masson G. Highly enantioselective electrophilic α-bromination of enecarbamates: chiral phosphoric acid and calcium phosphate salt catalysts. Journal of the American Chemical Society. 134: 10389-92. PMID 22686436 DOI: 10.1021/ja304095z |
0.33 |
|
2012 |
He L, Bekkaye M, Retailleau P, Masson G. Chiral phosphoric acid catalyzed inverse-electron-demand aza-Diels-Alder reaction of isoeugenol derivatives. Organic Letters. 14: 3158-61. PMID 22671430 DOI: 10.1021/ol301251h |
0.493 |
|
2012 |
Dagousset G, Retailleau P, Masson G, Zhu J. Chiral phosphoric acid-catalyzed enantioselective three-component Povarov reaction using cyclic enethioureas as dienophiles: stereocontrolled access to enantioenriched hexahydropyrroloquinolines. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5869-73. PMID 22467440 DOI: 10.1002/Chem.201200523 |
0.507 |
|
2012 |
Courant T, Masson G. Photoredox-initiated α-alkylation of imines through a three-component radical/cationic reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 423-7. PMID 22161892 DOI: 10.1002/chem.201103062 |
0.339 |
|
2012 |
Bouma MJ, Masson G, Zhu J. Exploiting the divergent reactivity of isocyanoacetates: One-pot three-component synthesis of functionalized angular furoquinolines European Journal of Organic Chemistry. 475-479. DOI: 10.1002/Ejoc.201101567 |
0.407 |
|
2011 |
Dagousset G, Zhu J, Masson G. Chiral phosphoric acid-catalyzed enantioselective three-component Povarov reaction using enecarbamates as dienophiles: highly diastereo- and enantioselective synthesis of substituted 4-aminotetrahydroquinolines. Journal of the American Chemical Society. 133: 14804-13. PMID 21827206 DOI: 10.1021/Ja205891M |
0.508 |
|
2011 |
Denis JB, Masson G, Retailleau P, Zhu J. Cinchona alkaloid amide catalyzed enantioselective formal [2+2] cycloadditions of allenoates and imines: synthesis of 2,4-disubstituted azetidines. Angewandte Chemie (International Ed. in English). 50: 5356-60. PMID 21538745 DOI: 10.1002/Anie.201100706 |
0.438 |
|
2011 |
Lalli C, Bouma MJ, Bonne D, Masson G, Zhu J. Exploiting the divergent reactivity of α-isocyanoacetate: multicomponent synthesis of 5-alkoxyoxazoles and related heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 880-9. PMID 21226103 DOI: 10.1002/Chem.201002098 |
0.324 |
|
2011 |
Lalli C, Brioche J, Bernadat G, Masson G. Catalytic enantioselective cycloaddition with chiral lewis bases Current Organic Chemistry. 15: 4108-4127. DOI: 10.2174/138527211798109178 |
0.416 |
|
2011 |
Denis J-, Masson G, Retailleau P, Zhu J. Catalytic Asymmetric Synthesis of Disubstituted Azetidines Synfacts. 2011: 792-792. DOI: 10.1055/S-0030-1260629 |
0.395 |
|
2011 |
George N, Bekkaye M, Masson G, Zhu J. A practical, one-pot multicomponent synthesis of α-amidosulfides and their application as latent N-acylimines in the Friedel-Crafts reaction European Journal of Organic Chemistry. 3695-3699. DOI: 10.1002/Ejoc.201100426 |
0.393 |
|
2011 |
George N, Bekkaye M, Masson G, Zhu J. ChemInform Abstract: A Practical, One-Pot Multicomponent Synthesis of α-Amidosulfides and Their Application as Latent N-Acylimines in the Friedel-Crafts Reaction. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201147046 |
0.362 |
|
2011 |
Masson G, Zhu J. ChemInform Abstract: Asymmetric Morita-Baylis-Hillman Reaction and Its Aza Analogue Cheminform. 42: no-no. DOI: 10.1002/chin.201140202 |
0.423 |
|
2010 |
Bouma M, Masson G, Zhu J. Zinc chloride promoted formal oxidative coupling of aromatic aldehydes and isocyanides to alpha-ketoamides. The Journal of Organic Chemistry. 75: 2748-51. PMID 20302346 DOI: 10.1021/Jo100302Y |
0.368 |
|
2010 |
Abermil N, Masson G, Zhu J. Aza-Morita-Baylis-Hillman Reaction Using AliphaticImine Precursors Synfacts. 2010: 595-595. DOI: 10.1055/S-0029-1219744 |
0.383 |
|
2010 |
Abermil N, Masson G, Zhu J. ChemInform Abstract: Enantioselective Aza-Morita-Baylis-Hillman Reaction Using Aliphatic α-Amidosulfones as Imine Surrogates. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201029041 |
0.394 |
|
2010 |
Masson G, Neuville L, Zhu J. ChemInform Abstract: Development of Multicomponent and Domino Reactions Based on α-Isocyanoacetamide and 5-Aminooxazole Cheminform. 41. DOI: 10.1002/chin.201010233 |
0.33 |
|
2010 |
Abermil N, Masson G, Zhu J. Enantioselective Aza-morita-baylis-hillman reaction using aliphatic α-amidosulfones as imine surrogates Advanced Synthesis and Catalysis. 352: 656-660. DOI: 10.1002/Adsc.200900900 |
0.373 |
|
2009 |
Dagousset G, Drouet F, Masson G, Zhu J. Chiral Brønsted acid-catalyzed enantioselective multicomponent Mannich reaction: synthesis of anti-1,3-diamines using enecarbamates as nucleophiles. Organic Letters. 11: 5546-9. PMID 19886612 DOI: 10.1021/Ol9023985 |
0.489 |
|
2009 |
Yue T, Wang MX, Wang DX, Masson G, Zhu J. Catalytic asymmetric Passerini-type reaction: chiral aluminum-organophosphate-catalyzed enantioselective alpha-addition of isocyanides to aldehydes. The Journal of Organic Chemistry. 74: 8396-9. PMID 19788173 DOI: 10.1021/Jo9017765 |
0.432 |
|
2009 |
Abermil N, Masson G, Zhu J. Invertible enantioselectivity in 6'-deoxy-6'-acylamino-beta-isocupreidine-catalyzed asymmetric aza-Morita-Baylis-Hillman reaction: key role of achiral additive. Organic Letters. 11: 4648-51. PMID 19775129 DOI: 10.1021/Ol901920S |
0.375 |
|
2009 |
Yue T, Wang MX, Wang DX, Masson G, Zhu J. Brønsted acid catalyzed enantioselective three-component reaction involving the alpha addition of isocyanides to imines. Angewandte Chemie (International Ed. in English). 48: 6717-21. PMID 19658144 DOI: 10.1002/Anie.200902385 |
0.458 |
|
2009 |
Liu H, Dagousset G, Masson G, Retailleau P, Zhu J. Chiral Brønsted acid-catalyzed enantioselective three-component Povarov reaction. Journal of the American Chemical Society. 131: 4598-9. PMID 19334771 DOI: 10.1021/Ja900806Q |
0.492 |
|
2009 |
Fontaine P, Masson G, Zhu J. Synthesis of pyrroles by consecutive multicomponent reaction/[4 + 1] cycloaddition of alpha-iminonitriles with isocyanides. Organic Letters. 11: 1555-8. PMID 19320503 DOI: 10.1021/Ol9001619 |
0.469 |
|
2009 |
Wu YC, Bernadat G, Masson G, Couturier C, Schlama T, Zhu J. Synthetic studies on (-)-lemonomycin: an efficient asymmetric synthesis of lemonomycinone amide. The Journal of Organic Chemistry. 74: 2046-52. PMID 19196163 DOI: 10.1021/Jo8027449 |
0.46 |
|
2009 |
Wu Y-, Bernadat G, Masson G, Couturier C, Schlama T, Zhu J. Synthesis of Lemonomycinone Amide Synfacts. 2009: 1070-1070. DOI: 10.1055/S-0029-1217863 |
0.303 |
|
2009 |
Liu H, Dagousset G, Masson G, Retailleau P, Zhu J. Brønsted Acid Catalyzed Enantioselective Three-ComponentPovarov Reaction Synfacts. 2009: 681-681. DOI: 10.1055/S-0029-1216765 |
0.418 |
|
2009 |
Fontaine P, Masson G, Zhu J. Synthesis of 2-Aminopyrroles by Sequential MCR/[4+1] Cycloaddition Synfacts. 2009: 599-599. DOI: 10.1055/S-0029-1216712 |
0.338 |
|
2009 |
Masson G, Zhu J, Drouet F, Fontaine P. IBX/TBAB-Mediated Oxidation of Primary Amines to Nitriles Synthesis. 2009: 1370-1374. DOI: 10.1055/S-0028-1087994 |
0.381 |
|
2009 |
Liu H, Dagousset G, Masson G, Retailleau P, Zhu J. ChemInform Abstract: Chiral Broensted Acid Catalyzed Enantioselective Three-Component Povarov Reaction. Cheminform. 40. DOI: 10.1002/CHIN.200935149 |
0.472 |
|
2009 |
Abermil N, Masson G, Zhu J. ChemInform Abstract: Highly Enantioselective Aza Morita-Baylis-Hillman Reaction Catalyzed by Bifunctional β-Isocupreidine Derivatives. Cheminform. 40. DOI: 10.1002/CHIN.200905026 |
0.381 |
|
2008 |
Abermil N, Masson G, Zhu J. Highly enantioselective aza Morita-Baylis-Hillman reaction catalyzed by bifunctional beta-isocupreidine derivatives. Journal of the American Chemical Society. 130: 12596-7. PMID 18729367 DOI: 10.1021/Ja805122J |
0.4 |
|
2008 |
Fontaine P, Chiaroni A, Masson G, Zhu J. One-pot three-component synthesis of alpha-iminonitriles by IBX/TBAB-mediated oxidative Strecker reaction. Organic Letters. 10: 1509-12. PMID 18345680 DOI: 10.1021/Ol800199B |
0.498 |
|
2008 |
Grassot JM, Masson G, Zhu J. Synthesis of alpha-ketoamides by a molecular-sieves-promoted formal oxidative coupling of aliphatic aldehydes with isocyanides. Angewandte Chemie (International Ed. in English). 47: 947-50. PMID 18092314 DOI: 10.1002/Anie.200704840 |
0.404 |
|
2008 |
Masson G, Zhu J, Abermil N. Catalytic Asymmetric Morita-Baylis-Hillman Reactions of Imines Synfacts. 2008: 1215-1215. DOI: 10.1055/S-0028-1083391 |
0.436 |
|
2008 |
Fontaine P, Chiaroni A, Masson G, Zhu J. ChemInform Abstract: One-Pot Three-Component Synthesis of α-Iminonitriles by IBX/TBAB-Mediated Oxidative Strecker Reaction Cheminform. 39. DOI: 10.1002/CHIN.200836081 |
0.375 |
|
2007 |
Pirali T, Tron GC, Masson G, Zhu J. Ammonium chloride promoted three-component synthesis of 5-iminooxazoline and its subsequent transformation to macrocyclodepsipeptide. Organic Letters. 9: 5275-8. PMID 17990892 DOI: 10.1021/Ol7024372 |
0.342 |
|
2007 |
Masson G, Housseman C, Zhu J. The enantioselective Morita-Baylis-Hillman reaction and its aza counterpart. Angewandte Chemie (International Ed. in English). 46: 4614-28. PMID 17397122 DOI: 10.1002/Anie.200604366 |
0.4 |
|
2006 |
Masson G, Den Hartog T, Schoemaker HE, Hiemstra H, Van Maarseveen JH. Intramolecular staudinger ligation towards biaryl-containing lactams Synlett. 865-868. DOI: 10.1055/S-2006-939059 |
0.33 |
|
2006 |
Masson G, den Hartog T, Schoemaker HE, Hiemstra H, van Maarseveen JH. Intramolecular Staudinger Ligation Towards Biaryl-Containing Lactams. Cheminform. 37. DOI: 10.1002/chin.200631155 |
0.307 |
|
2002 |
Godin G, Compain P, Masson G, Martin OR. A general strategy for the practical synthesis of nojirimycin C-glycosides and analogues. Extension to the first reported example of an iminosugar 1-phosphonate. The Journal of Organic Chemistry. 67: 6960-70. PMID 12353989 DOI: 10.1021/Jo0203903 |
0.618 |
|
2000 |
Masson G, Compain P, Martin OR. A new, stereocontrolled approach to iminosugar C-glycosides from L-sorbose. Organic Letters. 2: 2971-4. PMID 10986085 DOI: 10.1021/OL0062493 |
0.572 |
|
Show low-probability matches. |