Literature DB >> 25488620

Diazo compounds in continuous-flow technology.

Simon T R Müller1, Thomas Wirth.   

Abstract

Diazo compounds are very versatile reagents in organic chemistry and meet the challenge of selective assembly of structurally complex molecules. Their leaving group is dinitrogen; therefore, they are very clean and atom-efficient reagents. However, diazo compounds are potentially explosive and extremely difficult to handle on an industrial scale. In this review, it is discussed how continuous flow technology can help to make these powerful reagents accessible on large scale. Microstructured devices can improve heat transfer greatly and help with the handling of dangerous reagents safely. The in situ formation and subsequent consumption of diazo compounds are discussed along with advances in handling diazomethane and ethyl diazoacetate. The potential large-scale applications of a given methodology is emphasized.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  continuous flow; diazo compounds; green chemistry; microreactors; multistep synthesis

Mesh:

Substances:

Year:  2014        PMID: 25488620     DOI: 10.1002/cssc.201402874

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  11 in total

1.  Lab-scale production of anhydrous diazomethane using membrane separation technology.

Authors:  Doris Dallinger; C Oliver Kappe
Journal:  Nat Protoc       Date:  2017-09-14       Impact factor: 13.491

2.  A Versatile Room-Temperature Route to Di- and Trisubstituted Allenes Using Flow-Generated Diazo Compounds.

Authors:  Jian-Siang Poh; Duc N Tran; Claudio Battilocchio; Joel M Hawkins; Steven V Ley
Journal:  Angew Chem Int Ed Engl       Date:  2015-05-26       Impact factor: 15.336

3.  Development of a continuous process for α-thio-β-chloroacrylamide synthesis with enhanced control of a cascade transformation.

Authors:  Olga C Dennehy; Valérie M Y Cacheux; Benjamin J Deadman; Denis Lynch; Stuart G Collins; Humphrey A Moynihan; Anita R Maguire
Journal:  Beilstein J Org Chem       Date:  2016-11-24       Impact factor: 2.883

4.  A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl-Alkyl Cross-Coupling Reactions.

Authors:  Andreas Greb; Jian-Siang Poh; Stephanie Greed; Claudio Battilocchio; Patrick Pasau; David C Blakemore; Steven V Ley
Journal:  Angew Chem Int Ed Engl       Date:  2017-12-05       Impact factor: 15.336

5.  An autonomous organic reaction search engine for chemical reactivity.

Authors:  Vincenza Dragone; Victor Sans; Alon B Henson; Jaroslaw M Granda; Leroy Cronin
Journal:  Nat Commun       Date:  2017-06-09       Impact factor: 14.919

6.  Continuous-flow retro-Diels-Alder reaction: an efficient method for the preparation of pyrimidinone derivatives.

Authors:  Imane Nekkaa; Márta Palkó; István M Mándity; Ferenc Fülöp
Journal:  Beilstein J Org Chem       Date:  2018-02-01       Impact factor: 2.883

7.  Development and Scale-up of the Rapid Synthesis of Triphenyl Phosphites in Continuous Flow.

Authors:  Mengmei Mao; Le Zhang; Hanlin Yao; Li Wan; Zhong Xin
Journal:  ACS Omega       Date:  2020-04-17

Review 8.  Flow Biocatalysis: A Challenging Alternative for the Synthesis of APIs and Natural Compounds.

Authors:  Micol Santi; Luca Sancineto; Vanessa Nascimento; Juliano Braun Azeredo; Erika V M Orozco; Leandro H Andrade; Harald Gröger; Claudio Santi
Journal:  Int J Mol Sci       Date:  2021-01-20       Impact factor: 5.923

9.  In situ epoxide generation by dimethyldioxirane oxidation and the use of epichlorohydrin in the flow synthesis of a library of β-amino alcohols.

Authors:  Peter J Cossar; Jennifer R Baker; Nicholas Cain; Adam McCluskey
Journal:  R Soc Open Sci       Date:  2018-04-04       Impact factor: 2.963

10.  The Concept of Chemical Generators: On-Site On-Demand Production of Hazardous Reagents in Continuous Flow.

Authors:  Doris Dallinger; Bernhard Gutmann; C Oliver Kappe
Journal:  Acc Chem Res       Date:  2020-06-16       Impact factor: 22.384

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