Number of the records: 1
Meta-arylation of calixarenes using organomercurial chemistry
- 1.0397520 - FZÚ 2014 RIV GB eng J - Journal Article
Slavík, P. - Flídrová, K. - Dvořáková, H. - Eigner, Václav - Lhoták, P.
Meta-arylation of calixarenes using organomercurial chemistry.
Organic & Biomolecular Chemistry. Roč. 11, č. 33 (2013), s. 5528-5534. ISSN 1477-0520. E-ISSN 1477-0539
Grant - others:AV ČR(CZ) AP0701
Program: Akademická prémie - Praemium Academiae
Institutional support: RVO:68378271
Keywords : calix[4]arenes * mercuration * meta-substitution * supramolecular chemistry * jana2006
Subject RIV: CC - Organic Chemistry
Impact factor: 3.487, year: 2013
A direct mercuration reaction combined with a subsequent Pd-catalyzed arylation was used to introduce the aryl moiety into the meta position of the calix[4]arene skeleton. The application of organomercurial intermediates thus allows the straightforward formation of meta-aryl-substituted derivatives representing a unique substitution pattern in calixarene chemistry.
Permanent Link: http://hdl.handle.net/11104/0225133
Number of the records: 1