نمایش مختصر رکورد

dc.contributor.authorAdjibodéa, Steeve M.en_US
dc.contributor.authorKasséhin, Urbain C.en_US
dc.contributor.authorGbaguidi, Fernand A.en_US
dc.contributor.authorPoupaert, Jacques H.en_US
dc.date.accessioned1399-07-08T17:14:51Zfa_IR
dc.date.accessioned2020-09-29T17:14:51Z
dc.date.available1399-07-08T17:14:51Zfa_IR
dc.date.available2020-09-29T17:14:51Z
dc.date.issued2020-01-01en_US
dc.date.issued1398-10-11fa_IR
dc.date.submitted2019-03-06en_US
dc.date.submitted1397-12-15fa_IR
dc.identifier.citationAdjibodéa, Steeve M., Kasséhin, Urbain C., Gbaguidi, Fernand A., Poupaert, Jacques H.. (2020). Synthesis of icosadeuterio-benzopinacol (benzopinacol-d20). Journal of Medicinal and Chemical Sciences, 3(1), 35-40. doi: 10.26655/JMCHEMSCI.2020.1.4en_US
dc.identifier.issn2651-4702
dc.identifier.urihttps://dx.doi.org/10.26655/JMCHEMSCI.2020.1.4
dc.identifier.urihttp://www.jmchemsci.com/article_89436.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/16426
dc.description.abstractThis work reports on synthesis of high yield (92%) of isosadeuterio-benzopinacol (benzopinacol-d20) <em>via</em> photo-reductive dimerization of benzophenone-d10. The latter compound was obtained using an improved method to achieve a material with high isotopic purity (> 99%). This material can be served for calibration of Mass spectrometric assays. In this study, it was also observed that benzophenone-d10 reacts faster than its natural abundance counterpart. However, elucidating the origin of this phenomenon will require additional work.en_US
dc.format.extent676
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSami Publishing Company (SPC)en_US
dc.relation.ispartofJournal of Medicinal and Chemical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.26655/JMCHEMSCI.2020.1.4
dc.subjectbenzopinacol-d20en_US
dc.subjectbenzophenone-d10en_US
dc.subjectdimerizationen_US
dc.subjectphoto-reductiveen_US
dc.subjectPhotochemistryen_US
dc.titleSynthesis of icosadeuterio-benzopinacol (benzopinacol-d20)en_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentMedicinal Organic Chemistry Laboratory (MOCL), School of Pharmacy, Faculté des Sciences de la Santé, Universitéd'Abomey-Calavi, Campus du Champ de Foire, 01 BP 188, Cotonou, Béninen_US
dc.contributor.departmentMedicinal Organic Chemistry Laboratory (MOCL), School of Pharmacy, Faculté des Sciences de la Santé, Universitéd'Abomey-Calavi, Campus du Champ de Foire, 01 BP 188, Cotonou, Béninen_US
dc.contributor.departmentMedicinal Organic Chemistry Laboratory (MOCL), School of Pharmacy, Faculté des Sciences de la Santé, Universitéd'Abomey-Calavi, Campus du Champ de Foire, 01 BP 188, Cotonou, Béninen_US
dc.contributor.departmentMedicinal Chemistry (CMFA), Louvain Drug Research Institute, UCLouvain. 73, B1.73.10Av. E. Mounier B-1200 Brussels, Belgium, E.U.en_US
dc.citation.volume3
dc.citation.issue1
dc.citation.spage35
dc.citation.epage40


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