Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56989
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorDolnapa Yamanoen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.date.accessioned2018-09-05T03:33:15Z-
dc.date.available2018-09-05T03:33:15Z-
dc.date.issued2017-04-21en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-85011632872en_US
dc.identifier.other10.1055/s-0036-1588941en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011632872&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56989-
dc.description.abstract© Georg Thieme Verlag Stuttgart New York. Ph3P/I2-Et3N-mediated one-pot two-step esterification-cyclization toward 3-aryl coumarins and 3-aryl-4-methylcoumarins is reported. The reaction of a variety of aryl acetic acids containing steric or reactive group with 2-hydroxybenzaldehydes or 2′-hydroxyacetophenone proceeded smoothly at room temperature to afford the corresponding products in good to excellent yields using inexpensive and readily available reactants and reagents.en_US
dc.subjectChemistryen_US
dc.titlePh<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarinsen_US
dc.typeJournalen_US
article.title.sourcetitleSynletten_US
article.volume28en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.