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- Publisher Website: 10.1021/ja065572j
- Scopus: eid_2-s2.0-33845327559
- PMID: 17131986
- WOS: WOS:000242367000003
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Article: Template-directed one-step synthesis of cyclic trimers by ADMET
Title | Template-directed one-step synthesis of cyclic trimers by ADMET |
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Authors | |
Issue Date | 2006 |
Citation | Journal of the American Chemical Society, 2006, v. 128, n. 48, p. 15358-15359 How to Cite? |
Abstract | A trifurcated template, containing three secondary dialkylammonium ion recognition sites for encirclement by a dibenzo [24]crown-8-containing acyclic diene, is used to promote acyclic diene metatheses (ADMET) catalyzed by ruthenium-alkylidene complexes, affording a cyclic trimer in 55% yield. Following this one-step, threefold ADMET reaction, the resulting cyclic trimer was isolated by preparative HPLC and characterized by NMR spectroscopy and mass spectrometry. Copyright © 2006 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/332713 |
ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hou, Hongyi | - |
dc.contributor.author | Leung, Ken C.F. | - |
dc.contributor.author | Lanari, Daniela | - |
dc.contributor.author | Nelson, Alshakim | - |
dc.contributor.author | Stoddart, J. Fraser | - |
dc.contributor.author | Grubbs, Robert H. | - |
dc.date.accessioned | 2023-10-06T05:13:41Z | - |
dc.date.available | 2023-10-06T05:13:41Z | - |
dc.date.issued | 2006 | - |
dc.identifier.citation | Journal of the American Chemical Society, 2006, v. 128, n. 48, p. 15358-15359 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | http://hdl.handle.net/10722/332713 | - |
dc.description.abstract | A trifurcated template, containing three secondary dialkylammonium ion recognition sites for encirclement by a dibenzo [24]crown-8-containing acyclic diene, is used to promote acyclic diene metatheses (ADMET) catalyzed by ruthenium-alkylidene complexes, affording a cyclic trimer in 55% yield. Following this one-step, threefold ADMET reaction, the resulting cyclic trimer was isolated by preparative HPLC and characterized by NMR spectroscopy and mass spectrometry. Copyright © 2006 American Chemical Society. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of the American Chemical Society | - |
dc.title | Template-directed one-step synthesis of cyclic trimers by ADMET | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ja065572j | - |
dc.identifier.pmid | 17131986 | - |
dc.identifier.scopus | eid_2-s2.0-33845327559 | - |
dc.identifier.volume | 128 | - |
dc.identifier.issue | 48 | - |
dc.identifier.spage | 15358 | - |
dc.identifier.epage | 15359 | - |
dc.identifier.isi | WOS:000242367000003 | - |