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Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex

Gobbo P
•
Romagnoli T
•
Barbon SM
altro
Workentin MS
2015
  • journal article

Periodico
CHEMICAL COMMUNICATIONS
Abstract
A protection-deprotection strategy for strained alkynes used for bioorthogonal chemistry is reported. A strained alkyne can be protected with dicobalt-octacarbonyl and we demonstrate for the first time that a strained alkyne can be re-formed and isolated under mild reaction conditions for further bioorthogonal reactivity. The protection-deprotection strategy herein reported will expand the versatility of strained alkynes for the preparation of substrates in chemical biology and materials applications.
DOI
10.1039/c5cc01522g
WOS
WOS:000352269000045
Archivio
http://hdl.handle.net/11368/3004394
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84926442488
Diritti
metadata only access
google-scholar
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