Literature DB >> 17315058

Advanced organic synthesis using microreactor technology.

Batoul Ahmed-Omer1, Johan C Brandt, Thomas Wirth.   

Abstract

Organic synthesis in microreactors is a novel way of performing reactions in a highly controlled way. The benefits of microreactors result from their physical properties, such as enhanced mass and heat transfer as well as regular flow profiles leading to improved yields with increased selectivities.

Year:  2006        PMID: 17315058     DOI: 10.1039/b615072a

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


  19 in total

1.  Integrated Microfluidic Reactors.

Authors:  Wei-Yu Lin; Yanju Wang; Shutao Wang; Hsian-Rong Tseng
Journal:  Nano Today       Date:  2009-12       Impact factor: 20.722

2.  A flow-microreactor approach to protecting-group-free synthesis using organolithium compounds.

Authors:  Heejin Kim; Aiichiro Nagaki; Jun-ichi Yoshida
Journal:  Nat Commun       Date:  2011       Impact factor: 14.919

3.  Rapid catalyst screening by a continuous-flow microreactor interfaced with ultra-high-pressure liquid chromatography.

Authors:  Hui Fang; Qing Xiao; Fanghui Wu; Paul E Floreancig; Stephen G Weber
Journal:  J Org Chem       Date:  2010-08-20       Impact factor: 4.354

4.  Continuous flow based catch and release protocol for the synthesis of alpha-ketoesters.

Authors:  Alessandro Palmieri; Steven V Ley; Anastasios Polyzos; Mark Ladlow; Ian R Baxendale
Journal:  Beilstein J Org Chem       Date:  2009-05-20       Impact factor: 2.883

5.  An integrated microfluidic device for large-scale in situ click chemistry screening.

Authors:  Yanju Wang; Wei-Yu Lin; Kan Liu; Rachel J Lin; Matthias Selke; Hartmuth C Kolb; Nangang Zhang; Xing-Zhong Zhao; Michael E Phelps; Clifton K F Shen; Kym F Faull; Hsian-Rong Tseng
Journal:  Lab Chip       Date:  2009-06-17       Impact factor: 6.799

6.  Heterogeneously Catalyzed Continuous-Flow Hydrogenation Using Segmented Flow in Capillary Columns.

Authors:  Jasper J W Bakker; Martijn M P Zieverink; Raf W E G Reintjens; Freek Kapteijn; Jacob A Moulijn; Michiel T Kreutzer
Journal:  ChemCatChem       Date:  2011-06-09       Impact factor: 5.686

7.  Homocoupling of aryl halides in flow: Space integration of lithiation and FeCl(3) promoted homocoupling.

Authors:  Aiichiro Nagaki; Yuki Uesugi; Yutaka Tomida; Jun-Ichi Yoshida
Journal:  Beilstein J Org Chem       Date:  2011-08-02       Impact factor: 2.883

8.  The application of a monolithic triphenylphosphine reagent for conducting Appel reactions in flow microreactors.

Authors:  Kimberley A Roper; Heiko Lange; Anastasios Polyzos; Malcolm B Berry; Ian R Baxendale; Steven V Ley
Journal:  Beilstein J Org Chem       Date:  2011-12-08       Impact factor: 2.883

9.  Acid-mediated reactions under microfluidic conditions: a new strategy for practical synthesis of biofunctional natural products.

Authors:  Katsunori Tanaka; Koichi Fukase
Journal:  Beilstein J Org Chem       Date:  2009-08-20       Impact factor: 2.883

10.  The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow.

Authors:  Kimberley A Roper; Malcolm B Berry; Steven V Ley
Journal:  Beilstein J Org Chem       Date:  2013-09-02       Impact factor: 2.883

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.