Journal
DALTON TRANSACTIONS
Volume 41, Issue 33, Pages 9852-9854Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt30502j
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- Alexander von Humboldt Foundation
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A 1,3-dipolar cycloaddition reaction taking place quantitatively between propiolic acid guests and azide functions previously attached to binding sites within the cavity of a {Mo-132}-type Keplerate reproducibly gives a 2 : 1 ratio of 1,4- and 1,5-triazoles.
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