Examples of published literature for Solid supported

Transaminase‐catalyzed continuous synthesis of biogenic aldehydes

Martina L. Contente a, Francesca Paradisi *a,b

  • a School of Chemistry, University of Nottingham, University Park, Nottingham, NG7, 2RD, United Kingdom
  • b Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, 3012 Bern
View abstract

Bioprocess Intensification Using Flow Reactors: Stereoselective Oxidation of Achiral 1,3-diols with Immobilized Acetobacter Aceti

Valerio De Vitis 1, Federica Dall’Oglio 2, Francesca Tentori 3, Martina Letizia Contente 4, Elisabetta Brenna 3, Lucia Tamborini 2, Francesco Molinari 1

  • 1 Department of Food, Environmental and Nutritional Sciences (DeFENS), Università degli Studi di Milano, Via Celoria 2, 20133 Milan, Italy
  • 2 Department of Pharmaceutical Sciences (DISFARM), Università degli Studi di Milano, Via Mangiagalli 25, 20133 Milan, Italy
  • 3 Dipartimento di Chimica, Materiali ed Ingegneria Chimica “Giulio Natta” Politecnico di Milano, Via Mancinelli 7, I-20131 Milan, Italy
  • 4 School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK
View abstract

A solid-supported arylboronic acid catalyst for direct amidation

Yihao Dua,, Thomas Barbera,, Sol Ee Lima,, Henry S. Rzepab,, Ian R. Baxendale*a,, Andrew Whiting*a,

  • a Centre for Sustainable Chemical Processes, Department of Chemistry, Durham University, Science Laboratories, South Road, Durham, UK
  • a Department of Chemistry, Imperial College, South Kensington Campus, London, UK
View abstract

Novel Polystyrene-Immobilized Chiral Amino Alcohols as Heterogeneous Ligands for the Enantioselective Arylation of Aldehydes in Batch and Continuous Flow Regime

José AugustoForni, Luiz Fernando Toneto, Novaes, Renan Galaverna, Julio C.Pastre

  • Institute of Chemistry, University of Campinas – UNICAMP, PO Box 6154, 13083-970, Campinas, SP, Brazil
View abstract

Fine chemical syntheses under flow using SiliaCat catalysts

Rosaria Ciriminna a, Valerica Pandarus b, François Béland *b, Mario Pagliaro *a

  • * Corresponding authors a Istituto per lo Studio dei Materiali Nanostrutturati, CNR, via U. La Malfa 153, 90146 Palermo, Italy
  • b SiliCycle, 2500, Parc-Technologique Blvd, Québec, G1P 4S6 Canada
View abstract

A Flow-based Synthesis of Telmisartan

Alex Martin, Ali Siamaki, Katherine Belecki, B. Gupton

  • Department of Chemistry and Department of Chemical and Life Science Engineering Virginia Commonwealth University 601 W. Main St. Richmond Virginia 23284 United States
View abstract

Flow Synthesis of 2-Methylpyridines via α-Methylation

Camille Manansala1, Geoffrey K. Tranmer1 2 *

  • 1 College of Pharmacy, Faculty of Health Science, University of Manitoba, Winnipeg, MB R3E 0T6, Canada
  • 2 Department of Chemistry, Faculty of Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada
View abstract

Flow Alkylation of Thiols, Phenols, and Amines Using a Heterogenous Base in a Packed-Bed Reactor

Alastair Baker1, Michael Graz2, Robert Saunders2, Gareth J. S. Evans2, Ilaria Pitotti1 Thomas Wirth1

  • 1 School of Chemistry, Cardiff University, Park Place, Main Building, Cardiff CF10 3AT, UK
  • 2 Neem Biotech, Willowbrook Technical Units, Llandogo Road, St. Mellons, Cardiff CF3 0EF, UK
View abstract

Generation and Trapping of Ketenes in Flow

Cyril Henry1, David Bolien1, Bogdan Ibanescu1, Sally Bloodworth1, David C. Harrowven1, Xunli Zhang2, Andy Craven3, Helen F. Sneddon3, Richard J. Whitby1 *

  • 1 Chemistry, University of Southampton, Southampton, HANTS, SO17 1BJ, UK,
  • 2 Bioengineering Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, HANTS, SO17 1BJ, UK
  • 3 GlaxoSmithKline R&D Ltd., Medicines Research Centre, Gunnels Wood Road, Stevenage, HERTS, SG1 2NY, UK
View abstract

A monolith immobilised iridium Cp* catalyst for hydrogen transfer reactions under flow conditions

Maria Victoria Rojo* 1, Lucie Guetzoyan1, Ian. R. Baxendale1 2

  • 1 Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, UK
  • 2 Department of Chemistry, University of Durham, South Road, Durham, UK
View abstract

Facilitating Biomimetic Syntheses of Borrerine Derived Alkaloids by Means of Flow-Chemical Methods

Sonja B. KamptmannA, Steven V. Ley

  • A Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK
View abstract

Application Notes regarding Solid supported

Application Note 58 – Visible light singlet oxygen

Application note 58 Singlet Oxygen

In this application, the conversion of α-terpinene to ascaridole was used to indirectly detect the formation of singlet oxygen in continuous flow. The production of singlet oxygen in continuous flow was optimised using the two methods, and the heterogeneous photocatalyst stability was investigated. Once optimised, the singlet oxygen was used for the aerobic oxidation of boronic acids to phenols, and to degrade two environmental pollutants: bis-phenol A and cimetidine.

This application note describes:

  • Production of singlet oxygen in continuous flow
  • The use of the UV-150 photochemical reactor for heterogeneous dispersions
  • Use of heterogeneous photocatalysts as slurries and packed beds in continuous flow
  • Easy handling of a complex flow stream of solid, liquid and gas
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