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Martin G. Banwell

Researcher Next ID · RN-032607

Researcher · Chemistry

Jinan University

Guangzhou, France

Accepting doctoral researchersFunding unknown
Works count
1,204
Citation count
9,097
H-index
45
i10-index
276

Research interests

Chemistry
Materials Science
Crystallization and Solubility Studies
X-ray Diffraction in Crystallography
Chemical synthesis and alkaloids
Synthetic Organic Chemistry Methods
Crystallography and molecular interactions

Publications

  • Sucrose fatty acid esters: synthesis, emulsifying capacities, biological activities and structure-property profiles

    Critical Reviews in Food Science and Nutrition · 2020 · 10.1080/10408398.2020.1798346

  • The Palladium-Catalyzed Ullmann Cross-Coupling Reaction: A Modern Variant on a Time-Honored Process

    Accounts of Chemical Research · 2018 · 10.1021/acs.accounts.8b00169

  • Experimental demonstration of pH-dependent electrostatic catalysis of radical reactions

    Chemical Science · 2015 · 10.1039/c5sc01307k

  • The Au(I)-Catalyzed Intramolecular Hydroarylation of Terminal Alkynes Under Mild Conditions: Application to the Synthesis of 2H-Chromenes, Coumarins, Benzofurans, and Dihydroquinolines

    The Journal of Organic Chemistry · 2009 · 10.1021/jo902032p

  • Palladium‐Catalysed Cross‐Coupling and Related Reactions Involving Pyrroles

    European Journal of Organic Chemistry · 2006 · 10.1002/ejoc.200500911

  • Synthesis of Quinolines, 2-Quinolones, Phenanthridines, and 6(5H)-Phenanthridinones via Palladium[0]-Mediated Ullmann Cross-Coupling of 1-Bromo-2-nitroarenes with β-Halo-enals, -enones, or -esters

    Organic Letters · 2004 · 10.1021/ol0490375

  • Synthesis of Indoles via Palladium[0]-Mediated Ullmann Cross-Coupling of o-Halonitroarenes with α-Halo-enones or -enals

    Organic Letters · 2003 · 10.1021/ol034745w

  • Chemoenzymatic methods for the enantioselective preparation of sesquiterpenoid natural products from aromatic precursors

    Pure and Applied Chemistry · 2003 · 10.1351/pac200375020223

  • Convergent total synthesis of lamellarin K†

    Chemical Communications · 1997 · 10.1039/a705874h

  • Trifluoromethanesulfonic anhydride–4-(N,N-dimethylamino)pyridine as a reagent combination for effecting Bischler–Napieraiski cyclisation under mild conditions: application to total syntheses of the Amaryllidaceae alkaloids N-methylcrinasiadine, anhydrolycorinone, hippadine and oxoassoanine

    Journal of the Chemical Society Chemical Communications · 1995 · 10.1039/c39950002551

  • Oxidation of vicinal diols to .alpha.-dicarbonyl compounds by trifluoroacetic anhydride-activated dimethyl sulfoxide

    The Journal of Organic Chemistry · 1987 · 10.1021/jo00231a005

Current projects

    No projects listed.