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DC Field | Value | Language |
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dc.contributor.author | Kullapa Chanawanno | en_US |
dc.contributor.author | Cole Holstrom | en_US |
dc.contributor.author | Victor N. Nemykin | en_US |
dc.contributor.author | Richard S. Herrick | en_US |
dc.contributor.author | Christopher J. Ziegler | en_US |
dc.date.accessioned | 2018-09-05T02:56:59Z | - |
dc.date.available | 2018-09-05T02:56:59Z | - |
dc.date.issued | 2016-01-01 | en_US |
dc.identifier.issn | 23656549 | en_US |
dc.identifier.other | 2-s2.0-85041963640 | en_US |
dc.identifier.other | 10.1002/slct.201601748 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85041963640&origin=inward | en_US |
dc.identifier.uri | http://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.subject | Chemistry | en_US |
dc.title | New 1,1’-Ferrocene Bis(sulfonyl) Reagents | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | ChemistrySelect | en_US |
article.volume | 1 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | University of Minnesota Duluth | en_US |
article.stream.affiliations | College of the Holy Cross | en_US |
article.stream.affiliations | University of Akron | en_US |
article.stream.affiliations | University of Manitoba | en_US |
Appears in Collections: | CMUL: Journal Articles |
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