Literature DB >> 18537209

Flash chemistry: fast chemical synthesis by using microreactors.

Jun-ichi Yoshida1, Aiichiro Nagaki, Takeshi Yamada.   

Abstract

This concept article provides a brief outline of the concept of flash chemistry for carrying out extremely fast reactions in organic synthesis by using microreactors. Generation of highly reactive species is one of the key elements of flash chemistry. Another important element of flash chemistry is the control of extremely fast reactions to obtain the desired products selectively. Fast reactions are usually highly exothermic, and heat removal is an important factor in controlling such reactions. Heat transfer occurs very rapidly in microreactors by virtue of a large surface area per unit volume, making precise temperature control possible. Fast reactions often involve highly unstable intermediates, which decompose very quickly, making reaction control difficult. The residence time can be greatly reduced in microreactors, and this feature is quite effective in controlling such reactions. For extremely fast reactions, kinetics often cannot be used because of the lack of homogeneity of the reaction environment when they are conducted in conventional reactors such as flasks. Fast mixing using micromixers solves such problems. The concept of flash chemistry has been successfully applied to various organic reactions including a) highly exothermic reactions that are difficult to control in conventional reactors, b) reactions in which a reactive intermediate easily decomposes in conventional reactors, c) reactions in which undesired byproducts are produced in the subsequent reactions in conventional reactors, and d) reactions whose products easily decompose in conventional reactors. The concept of flash chemistry can be also applied to polymer synthesis. Cationic polymerization can be conducted with an excellent level of molecular-weight control and molecular-weight distribution control.

Entities:  

Year:  2008        PMID: 18537209     DOI: 10.1002/chem.200800582

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  39 in total

1.  The flow synthesis of heterocycles for natural product and medicinal chemistry applications.

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Journal:  Mol Divers       Date:  2010-10-20       Impact factor: 2.943

2.  Visible-light photoredox catalysis in flow.

Authors:  Joseph W Tucker; Yuan Zhang; Timothy F Jamison; Corey R J Stephenson
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-16       Impact factor: 15.336

3.  The assembly and use of continuous flow systems for chemical synthesis.

Authors:  Joshua Britton; Timothy F Jamison
Journal:  Nat Protoc       Date:  2017-10-26       Impact factor: 13.491

Review 4.  Automating drug discovery.

Authors:  Gisbert Schneider
Journal:  Nat Rev Drug Discov       Date:  2017-12-15       Impact factor: 84.694

5.  Integrated Microfluidic Reactors.

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

6.  Development of an automated microfluidic reaction platform for multidimensional screening: reaction discovery employing bicyclo[3.2.1]octanoid scaffolds.

Authors:  John R Goodell; Jonathan P McMullen; Nikolay Zaborenko; Jason R Maloney; Chuan-Xing Ho; Klavs F Jensen; John A Porco; Aaron B Beeler
Journal:  J Org Chem       Date:  2009-08-21       Impact factor: 4.354

7.  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

8.  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

9.  Synthesis of unsymmetrically substituted biaryls via sequential lithiation of dibromobiaryls using integrated microflow systems.

Authors:  Aiichiro Nagaki; Naofumi Takabayashi; Yutaka Tomida; Jun-ichi Yoshida
Journal:  Beilstein J Org Chem       Date:  2009-04-29       Impact factor: 2.883

10.  Oxidative cyclization of alkenols with oxone using a miniflow reactor.

Authors:  Yoichi M A Yamada; Kaoru Torii; Yasuhiro Uozumi
Journal:  Beilstein J Org Chem       Date:  2009-04-29       Impact factor: 2.883

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