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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob06456h
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dc.titleIron-catalyzed ene-type propargylation of diarylethylenes with propargyl alcohols
dc.contributor.authorPeng, S.
dc.contributor.authorWang, L.
dc.contributor.authorWang, J.
dc.date.accessioned2014-10-16T08:32:14Z
dc.date.available2014-10-16T08:32:14Z
dc.date.issued2012-01-14
dc.identifier.citationPeng, S., Wang, L., Wang, J. (2012-01-14). Iron-catalyzed ene-type propargylation of diarylethylenes with propargyl alcohols. Organic and Biomolecular Chemistry 10 (2) : 225-228. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob06456h
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94109
dc.description.abstractThe diarylalkenyl propargylic complex framework has been found in many natural products and medicinal regents. Herein, we have disclosed an unprecedented FeCl 3 catalyzed ene-type reaction of propargylic alcohols with 1,1-diaryl alkenes which enabled us to furnish a diarylalkenyl propargylic complex framework in moderate to high chemical yields (up to 98%). © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1ob06456h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c1ob06456h
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume10
dc.description.issue2
dc.description.page225-228
dc.identifier.isiut000298555700002
Appears in Collections:Staff Publications

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