Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/52032
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dc.contributor.authorRachaneebhorn Inkumen_US
dc.contributor.authorAphiwat Teerawutgulragen_US
dc.contributor.authorPakawan Puangsombaten_US
dc.contributor.authorNuansri Rakariyathamen_US
dc.date.accessioned2018-09-04T06:16:00Z-
dc.date.available2018-09-04T06:16:00Z-
dc.date.issued2012-09-01en_US
dc.identifier.issn19057873en_US
dc.identifier.other2-s2.0-84867869116en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84867869116&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52032-
dc.description.abstractHerein, a simple synthesis pathway of beta-blockers starting from allyl amine is presented. This synthesis features the opening of an epoxide ring with phenol derivatives followed by N-alkylation with iso-propylbromide to produce racemic propranolol and atenolol. © 2012 by Maejo University, San Sai, Chiang Mai, 50290 Thailand.en_US
dc.subjectMultidisciplinaryen_US
dc.titleAn alternative synthesis of (+) - propranolol and (+) atenololen_US
dc.typeJournalen_US
article.title.sourcetitleMaejo International Journal of Science and Technologyen_US
article.volume6en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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