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Volumn 46, Issue 12, 2007, Pages 2101-2103

Isolation of a copper(I) triazolide: A "click" intermediate

Author keywords

Alkynes; Azides; Click chemistry; Copper; Cycloadditions; Reaction mechanisms

Indexed keywords

COMPLEXATION; COPPER; CYCLOADDITION; ORGANOMETALLICS;

EID: 34250883966     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604444     Document Type: Article
Times cited : (234)

References (37)
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    • For trapping of assumed copper(I) triazolide intermediates by electrophiles, see a) B. Gerard, J. Ryan, A. B. Beeler, J. A. Porco, Jr., Tetrahedron 2006, 62, 6405;
    • For trapping of assumed copper(I) triazolide intermediates by electrophiles, see a) B. Gerard, J. Ryan, A. B. Beeler, J. A. Porco, Jr., Tetrahedron 2006, 62, 6405;
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    • Cross experiments are in progress to rule out fast, reversible NHC dissociation, acetylide ligand exchange, and formation of dinuclear complexes
    • Cross experiments are in progress to rule out fast, reversible NHC dissociation, acetylide ligand exchange, and formation of dinuclear complexes.
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    • With a π-acceptor ligand instead of a strong donor ligand, such as an N-heterocyclic carbene, a coordination number of 3 at a 16-valence-electron copper complex would certainly be a viable alternative for intermediates in click catalysis
    • With a π-acceptor ligand instead of a strong donor ligand, such as an N-heterocyclic carbene, a coordination number of 3 at a 16-valence-electron copper complex would certainly be a viable alternative for intermediates in click catalysis.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.