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- Publisher Website: 10.1002/asia.201100457
- Scopus: eid_2-s2.0-80053496360
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Article: Reactions under the click chemistry philosophy employed in supramolecular and mechanostereochemical systems
| Title | Reactions under the click chemistry philosophy employed in supramolecular and mechanostereochemical systems |
|---|---|
| Authors | |
| Keywords | click chemistry cycloaddition mechanical bond supramolecular chemistry thiol additions |
| Issue Date | 2011 |
| Citation | Chemistry - An Asian Journal, 2011, v. 6, n. 10, p. 2660-2669 How to Cite? |
| Abstract | Supramolecular chemistry and mechanostereochemistry have been major beneficiaries of the concepts and reactions pioneered under the "click chemistry" philosophy. The success of the copper(I) 1,3-dipolar cycloaddition between azides and alkynes, resulting in the triazole ring has inspired the application of other emerging click reactions, for example, Diels-Alder cycloadditions, thiol-ene/yne chemistry, and nitrile N-oxide cycloadditions, towards the creation of advanced functional supramolecular and mechanostereochemical systems. In this Focus Review, recent advances in the use of click chemistry in these fields are highlighted. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| Persistent Identifier | http://hdl.handle.net/10722/332962 |
| ISSN | 2023 Impact Factor: 3.5 2023 SCImago Journal Rankings: 0.846 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Fahrenbach, Albert C. | - |
| dc.contributor.author | Stoddart, J. Fraser | - |
| dc.date.accessioned | 2023-10-06T05:15:40Z | - |
| dc.date.available | 2023-10-06T05:15:40Z | - |
| dc.date.issued | 2011 | - |
| dc.identifier.citation | Chemistry - An Asian Journal, 2011, v. 6, n. 10, p. 2660-2669 | - |
| dc.identifier.issn | 1861-4728 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/332962 | - |
| dc.description.abstract | Supramolecular chemistry and mechanostereochemistry have been major beneficiaries of the concepts and reactions pioneered under the "click chemistry" philosophy. The success of the copper(I) 1,3-dipolar cycloaddition between azides and alkynes, resulting in the triazole ring has inspired the application of other emerging click reactions, for example, Diels-Alder cycloadditions, thiol-ene/yne chemistry, and nitrile N-oxide cycloadditions, towards the creation of advanced functional supramolecular and mechanostereochemical systems. In this Focus Review, recent advances in the use of click chemistry in these fields are highlighted. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | - |
| dc.language | eng | - |
| dc.relation.ispartof | Chemistry - An Asian Journal | - |
| dc.subject | click chemistry | - |
| dc.subject | cycloaddition | - |
| dc.subject | mechanical bond | - |
| dc.subject | supramolecular chemistry | - |
| dc.subject | thiol additions | - |
| dc.title | Reactions under the click chemistry philosophy employed in supramolecular and mechanostereochemical systems | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1002/asia.201100457 | - |
| dc.identifier.scopus | eid_2-s2.0-80053496360 | - |
| dc.identifier.volume | 6 | - |
| dc.identifier.issue | 10 | - |
| dc.identifier.spage | 2660 | - |
| dc.identifier.epage | 2669 | - |
| dc.identifier.eissn | 1861-471X | - |
| dc.identifier.isi | WOS:000296273900008 | - |