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  1. Home ›
  2. Publication
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Fully automated sequence-specific synthesis of α-peptides using flow chemistry

Knudsen, K. R.; Ladlow, M.; Bandpey, Z.; Ley, S. V.; J. Flow Chem., 2014, 4(1), 18-21

Link to article

Flash carboxylation: fast lithiation-carboxylation sequence at room temperature in continuous flow

Pieber, B.; Glasnov, T.; Kappe, C. O.; RSC Adv., 2014, 4, 13430-13433

Link to article

Synthesis, anti‐tubulin and antiproliferative SAR of steroidomimetic dihydroisoquinolinones

Leese, M. P.; Jourdan, F. L.; Major, M. R.; Dohle, W.; Thomas, M. P.; Hamel, E.; Ferrandis, E.; Mahon, M. F.; Newman, S. P.; Purohit, A.; Potter, B. V. L.; ChemMedChem, 2014, 9, 798-812

Link to article

Systematic evaluation of the palladium-catalyzed hydrogenation under flow conditions

Hattori, T.; Tsubone, A.; Sawama, Y.; Monguchi, Y.; Sajiki, H.; Tetrahedron, 2014, 70(32), 4790-4798

Link to article

Chemistry of pyrrolizidine alkaloids revisited – semi-synthetic microwave and continuous-flow approaches toward Crotalaria-alkaloids

Martineza, S. T.; Pinto, A. C.; Glasnov, T.; Kappe, C. O.; Tetrahedron Letters, 2014, 55(30), 4181-4184

Link to article

Synthesis of an azabicyclic framework towards (±)-actinophyllic acid

Mortimer, D.; Whiting, M.; Harrity, J. P. A.; Jones, S.; Coldham, I.; Tetrahedron Letters, 2014, 55, 1255-1257

Link to article

Measurement of supramolecular effective molarities for intramolecular H-bonds in zinc porphyrin-imidazole complexes

Jinks, M. A.; Sun, H.; Hunter, C. A.; Org. Biomol. Chem., 2014, 12, 1440-1447

Link to article

Evaluating dynamic kinetic resolution strategies in the asymmetric hydrosilylation of cyclic ketimines

Jones, S.; Zhao, P.; Tetrahedron: Asymmetry, 2014, 25(3), 238-244

Link to article

Enantiomeric separation of bicyclo[2.2.2]octane‐based 2‐amino‐3‐carboxylic acids on macrocyclic glycopeptide chiral stationary phases

Pataj, Z.; Ilisz, I.; Grecso, N; Palko, M.; Fulop, F.; Armstrong, D. W.; Peter, A.; Chirality, 2014, 26, 200-208

Link to article

3‐Aminoazetidin‐2‐one derivatives as N‐acylethanolamine acid amidase (NAAA) inhibitors suitable for systemic administration

Fiasella, A.; Nuzzi, A.; Summa, M.; Armirotti, A.; Tarozzo, G.; Tarzia, G.; Mor, M.; Bertozzi, F.; Bandiera, T.; Piomelli, D.; ChemMedChem, 2014, 9(7), 1602-1614

Link to article

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