Please use this identifier to cite or link to this item: 192.168.6.56/handle/123456789/74970
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dc.contributor.editorJ. Witczak, Zbigniew-
dc.contributor.editorBielski, Roman-
dc.date.accessioned2019-07-03T06:17:05Z-
dc.date.available2019-07-03T06:17:05Z-
dc.date.issued2018-
dc.identifier.isbn978-3-319-65587-1-
dc.identifier.urihttp://10.6.20.12:80/handle/123456789/74970-
dc.descriptionConnecting molecular units exhibiting specific physical, chemical, or biological properties is a pivotal area of chemical synthesis. For many years, only organic units were considered worthy of this noble chemistry. Not anymore. Constructs containing inorganic or biological units are more and more common. The number of papers on coupling various moieties has been growing rapidly for dozens of years. The introduction of click chemistry was a game changer. Today, besides the original click process—the Huisgen reaction forming cyclic triazole—we have several other good coupling reactions such as the addition of thiols to various olefins, acetylenes, and isocyanates, Diels-Alder click reactions, and the newest one sulfur(VI) fluoride exchange (SuFex).en
dc.languageenen
dc.language.isoenen_US
dc.publisherSpringer International Publishing AGen_US
dc.subjectGlycosciencesen_US
dc.titleCoupling and Decoupling of Diverse Molecular Units in Glycosciencesen_US
dc.typeBooken_US
Appears in Collections:Chemistry

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