Literature DB >> 24763674

Continuous flow chemistry: a discovery tool for new chemical reactivity patterns.

Jan Hartwig1, Jan B Metternich, Nikzad Nikbin, Andreas Kirschning, Steven V Ley.   

Abstract

Continuous flow chemistry as a process intensification tool is well known. However, its ability to enable chemists to perform reactions which are not possible in batch is less well studied or understood. Here we present an example, where a new reactivity pattern and extended reaction scope has been achieved by transferring a reaction from batch mode to flow. This new reactivity can be explained by suppressing back mixing and precise control of temperature in a flow reactor set up.

Year:  2014        PMID: 24763674     DOI: 10.1039/c4ob00662c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  6 in total

1.  A methanol and protic ionic liquid Ugi multicomponent reaction path to cytotoxic α-phenylacetamido amides.

Authors:  Ahmed Al Otaibi; Fiona M Deane; Cecilia C Russell; Lacey Hizartzidis; Siobhann N McCluskey; Jennette A Sakoff; Adam McCluskey
Journal:  RSC Adv       Date:  2019-03-08       Impact factor: 4.036

2.  Real-time Monitoring of Reactions Performed Using Continuous-flow Processing: The Preparation of 3-Acetylcoumarin as an Example.

Authors:  Trevor A Hamlin; Nicholas E Leadbeater
Journal:  J Vis Exp       Date:  2015-11-18       Impact factor: 1.355

3.  Iterative reactions of transient boronic acids enable sequential C-C bond formation.

Authors:  Claudio Battilocchio; Florian Feist; Andreas Hafner; Meike Simon; Duc N Tran; Daniel M Allwood; David C Blakemore; Steven V Ley
Journal:  Nat Chem       Date:  2016-02-08       Impact factor: 24.427

Review 4.  Enabling Technologies for the Future of Chemical Synthesis.

Authors:  Daniel E Fitzpatrick; Claudio Battilocchio; Steven V Ley
Journal:  ACS Cent Sci       Date:  2016-02-24       Impact factor: 14.553

5.  Gas/Liquid-Phase Micro-Flow Trifluoromethylation using Fluoroform: Trifluoromethylation of Aldehydes, Ketones, Chalcones, and N-Sulfinylimines.

Authors:  Kazuki Hirano; Satoshi Gondo; Nagender Punna; Etsuko Tokunaga; Norio Shibata
Journal:  ChemistryOpen       Date:  2019-02-05       Impact factor: 2.911

6.  C(sp3 )-H Arylation Promoted by a Heterogeneous Palladium-N-Heterocyclic Carbene Complex in Batch and Continuous Flow.

Authors:  Francesco Ferlin; Ioannis Anastasiou; Nihad Salameh; Takeru Miyakoshi; Olivier Baudoin; Luigi Vaccaro
Journal:  ChemSusChem       Date:  2022-02-18       Impact factor: 9.140

  6 in total

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