Literature DB >> 22758402

Unprecedented meta-substitution of calixarenes: direct way to inherently chiral derivatives.

Petr Slavik1, Miroslav Dudic, Karolina Flidrova, Jan Sykora, Ivana Cisarova, Stanislav Böhm, Pavel Lhotak.   

Abstract

Electrophilic aromatic substitution in the calix[n]arene series is a well-established procedure leading exclusively to para-substituted derivatives. An unprecedented regioselectivity of the mercuration reaction leading to the meta-substituted calix[4]arenes is described. These compounds represent a new type of substitution pattern in classical calixarene chemistry and open the door for the straightforward synthesis of inherently chiral receptors based on calixarenes.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22758402     DOI: 10.1021/ol301420t

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Synthesis of upper rim-double-bridged calix[4]arenes bearing seven membered rings and related compounds.

Authors:  M Tlustý; V Eigner; M Babor; M Kohout; P Lhoták
Journal:  RSC Adv       Date:  2019-07-16       Impact factor: 4.036

2.  Attempted synthesis of a meta-metalated calix[4]arene.

Authors:  Christopher D Jurisch; Gareth E Arnott
Journal:  Beilstein J Org Chem       Date:  2019-08-22       Impact factor: 2.883

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.