Please use this identifier to cite or link to this item: https://doi.org/10.1039/c7sc00408g
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dc.titleReaction discovery using acetylene gas as the chemical feedstock accelerated by the "stop-flow" micro-tubing reactor system
dc.contributor.authorXue F.
dc.contributor.authorDeng H.
dc.contributor.authorXue C.
dc.contributor.authorMohamed D.K.B.
dc.contributor.authorTang K.Y.
dc.contributor.authorWu J.
dc.date.accessioned2020-09-09T01:20:27Z
dc.date.available2020-09-09T01:20:27Z
dc.date.issued2017
dc.identifier.citationXue F., Deng H., Xue C., Mohamed D.K.B., Tang K.Y., Wu J. (2017). Reaction discovery using acetylene gas as the chemical feedstock accelerated by the "stop-flow" micro-tubing reactor system. Chemical Science 8 (5) : 3623-3627. ScholarBank@NUS Repository. https://doi.org/10.1039/c7sc00408g
dc.identifier.issn20416520
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174900
dc.description.abstractAcetylene gas has been applied as a feedstock under transition-metal catalysis and photo-redox conditions to produce important chemicals including terminal alkynes, fulvenes, and fluorinated styrene compounds. The reaction discovery process was accelerated through the use of "stop-flow" micro-tubing reactors. This reactor prototype was developed by joining elements from both continuous micro-flow and conventional batch reactors, which was convenient and effective for gas/liquid reaction screening. Notably, the developed transformations were either inefficient or unsuccessful in conventional batch reactors. Its success relies on the unique advantages provided by this "stop-flow" micro-tubing reactor system. © 2017 The Royal Society of Chemistry.
dc.publisherRoyal Society of Chemistry
dc.sourceUnpaywall 20200831
dc.subjectAcetylene
dc.subjectFeedstocks
dc.subjectLighting
dc.subjectStyrene
dc.subjectTubing
dc.subjectAcetylene gas
dc.subjectChemical feedstocks
dc.subjectMicro-flow
dc.subjectReactor prototype
dc.subjectReactor systems
dc.subjectRedox condition
dc.subjectTerminal alkyne
dc.subjectTransition metal catalysis
dc.subjectBatch reactors
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c7sc00408g
dc.description.sourcetitleChemical Science
dc.description.volume8
dc.description.issue5
dc.description.page3623-3627
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