Reactions under the Click Chemistry Philosophy Employed in Supramolecular and Mechanostereochemical Systems

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Supramolecular chemistry and mechanostereo-chemistry have been major beneficiaries of the concepts and reactions pioneered under the "click chemistry" philosophy. The success of the copper(I) 1,3-dipolar cycloaddition between azides and alkynes, resulting in the triazole ring has inspired the application of other emerging click reactions, for example, Diels-Alder cycloadditions, thiolene/yne chemistry, and nitrile N-oxide cycloadditions, to-wards the creation of advanced functional supramolecular and mechanostereochemical systems. In this Focus Review, recent advances in the use of click chemistry in these fields are highlighted.
Publisher
WILEY-BLACKWELL
Issue Date
2011-10
Language
English
Article Type
Review
Keywords

DIELS-ALDER REACTION; MOLECULAR SHUTTLES; TEMPLATE SYNTHESIS; SHAPE-PERSISTENT; ROTAXANES; ION; CATALYSIS; TRIAZOLOPHANES; POLYROTAXANES; CYCLOADDITION

Citation

CHEMISTRY-AN ASIAN JOURNAL, v.6, no.10, pp.2660 - 2669

ISSN
1861-4728
DOI
10.1002/asia.201100457
URI
http://hdl.handle.net/10203/93994
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