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Volumn 53, Issue 7, 2014, Pages 1877-1880

Iridium-catalyzed intermolecular azide-alkyne cycloaddition of internal thioalkynes under mild conditions

Author keywords

click chemistry; cycloaddition; heterocycles; iridium; triazoles

Indexed keywords

AQUEOUS SOLVENTS; AZIDE-ALKYNE CYCLOADDITION; CLICK CHEMISTRY; CLICK REACTION; HETEROCYCLES; INTERNAL ALKYNES; MILD REACTION CONDITIONS; TRIAZOLES;

EID: 84893599212     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201309855     Document Type: Article
Times cited : (259)

References (64)
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    • During the preparation of our manuscript, an Ir-catalyzed AAC of bromoalkynes was reported (with mostly moderate efficiency).
    • During the preparation of our manuscript, an Ir-catalyzed AAC of bromoalkynes was reported (with mostly moderate efficiency):, E. Rasolofonjatovo, S. Theeramunkong, A. Bouriaud, S. Kolodych, M. Chaumontet, F. Taran, Org. Lett. 2013, 15, 4698-4701.
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    • To our knowledge, there is only one report that deals with the reaction of internal electron-rich alkynes under mild conditions.
    • To our knowledge, there is only one report that deals with the reaction of internal electron-rich alkynes under mild conditions:, B. C. Boren, S. Narayan, L. K. Rasmussen, L. Zhang, H. Zhao, Z. Lin, G. Jia, V. V. Fokin, J. Am. Chem. Soc. 2008, 130, 8923-8930.
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    • An iridium-azide complex in which the azide coordinates through the internal nitrogen is known.
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    • For a similar three-membered-ring iridium-sulfur interaction, see:, A. F. Dalebrook, L. J. Wright, Organometallics 2009, 28, 5536-5540.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.