C−H Bond Activation and Subsequent C−C Bond Formation Promoted by Osmium:  2-Vinylpyridine−Acetylene Couplings

2 pages, 2 scheme.

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PID https://www.doi.org/10.1021/ja060901t.s001
PID https://www.doi.org/10.1021/ja060901t
PID handle:10261/19496
URL https://pubs.acs.org/doi/pdf/10.1021/ja060901t
URL https://www.ncbi.nlm.nih.gov/pubmed/16594696
URL https://academic.microsoft.com/#/detail/2012173654
URL http://hdl.handle.net/10261/19496
URL http://dx.doi.org/10.1021/ja060901t
URL https://core.ac.uk/display/36030546
URL https://pubs.acs.org/doi/10.1021/ja060901t
URL https://figshare.com/articles/journal_contribution/C_H_Bond_Activation_and_Subsequent_C_C_Bond_Formation_Promoted_by_Osmium_2_Vinylpyridine_Acetylene_Couplings/3228247
URL http://digital.csic.es/handle/10261/19496
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Access Right Open Access
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Author Montserrat Olivan, 0000-0003-0381-0917
Author Enrique Oñate, 0000-0003-2094-719X
Author Miguel A. Esteruelas, 0000-0002-4829-7590
Author Francisco J. Fernández-Alvarez, 0000-0002-0497-1969
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Collected From Digital.CSIC; ORCID; figshare; Datacite; Crossref; Microsoft Academic Graph
Hosted By Journal of the American Chemical Society; Digital.CSIC; figshare
Publication Date 2006-03-18
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Country Spain
Description Complex OsH2Cl2(PiPr3)2 promotes the C−H activation of 2-vinylpyridine and subsequently couples the activated substrate with a second 2-vinylpyridine and two acetylene molecules. In the absence of 2-vinylpyridine, the activated substrate is coupled with an acetylene unit to afford a 2-butadienylpyridine derivative.
Description Financial support from the MEC of Spain (Project CTQ2005-00656) is acknowledged. F.J.F.-A. thanks CSIC and the European Social Fund for funding through the I3P Program.
Description Peer reviewed
Format 13824 bytes; application/vnd.ms-excel
Language English
Resource Type Other literature type; Article
system:type publication
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::fff38018fbbff9f415b61f4667ac46c7
Author jsonws_user
Last Updated 25 December 2020, 15:18 (CET)
Created 25 December 2020, 15:18 (CET)