Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55484
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dc.contributor.authorKullapa Chanawannoen_US
dc.contributor.authorCole Holstromen_US
dc.contributor.authorVictor N. Nemykinen_US
dc.contributor.authorRichard S. Herricken_US
dc.contributor.authorChristopher J. Ziegleren_US
dc.date.accessioned2018-09-05T02:56:59Z-
dc.date.available2018-09-05T02:56:59Z-
dc.date.issued2016-01-01en_US
dc.identifier.issn23656549en_US
dc.identifier.other2-s2.0-85041963640en_US
dc.identifier.other10.1002/slct.201601748en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85041963640&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55484-
dc.description.abstract© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Several new 1,1’-bis(sulfonyl)ferrocenes designed for the synthesis of sulfonamide linked biological conjugates have been prepared. 1,1’-Bis(sulfonylbromide)ferrocene can be produced from the corresponding sulfonylchloride via a bis(sulfonylhydrazide) intermediate. Bis(sulfonyl-N-hydroxybenzotriazole)ferrocene can also be synthesized from the sulfonyl chloride, and reaction of glycine methyl ester with the sulfonyl chloride affords a [3]ferrocenophane complex. All new compounds have been structurally characterized by X-ray crystallography.en_US
dc.subjectChemistryen_US
dc.titleNew 1,1’-Ferrocene Bis(sulfonyl) Reagentsen_US
dc.typeJournalen_US
article.title.sourcetitleChemistrySelecten_US
article.volume1en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Minnesota Duluthen_US
article.stream.affiliationsCollege of the Holy Crossen_US
article.stream.affiliationsUniversity of Akronen_US
article.stream.affiliationsUniversity of Manitobaen_US
Appears in Collections:CMUL: Journal Articles

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