Literature DB >> 21591617

Inherently chiral resorcin[4]arenes: a new concept for improving the functionality.

Sebastian Wiegmann1, Jochen Mattay.   

Abstract

A new reactive postion at the upper rim of inherently chiral resorcin[4]arenes was introduced through cleavage of an up to now unreactive methoxy group through the demethylating reagent 9-I-9-BBN. Conservation of the inherent chirality was warranted through the use of a protecting group at the free phenol group.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID： 21591617     DOI： 10.1021/ol200972w

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


  4 in total

1.  4,10,16,22-Tetra-kis(2-chloro-acet-oxy)-6,12,18,24-tetra-meth-oxy-2,8,14,20-tetra-pentyl-resorcin[4]arene.

Authors:  Pramod B Pansuriya; Holger B Friedrich; Glenn E M Maguire
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-10-12

2.  6,12,18,24-Tetra-meth-oxy-4,10,16,22-tetra-kis-[(meth-oxy-carbon-yl)meth-oxy]-2,8,14,20-tetra-kis-(2-phenyl-eth-yl)resorcin[4]arene.

Authors:  Pramod B Pansuriya; Holger B Friedrich; Glenn E M Maguire
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-12-10

3.  Synthesis of a coumarin derivative of resorcin[4]arene with solvent-controlled chirality.

Authors:  Anna Szafraniec; Waldemar Iwanek
Journal:  RSC Adv       Date:  2020-03-30       Impact factor: 3.361

4.  Enaminone Substituted Resorcin[4]arene-Sealing of an Upper-Rim with a Directional System of Hydrogen-Bonds.

Authors:  Anna Szafraniec; Marcin Grajda; Hanna Jędrzejewska; Agnieszka Szumna; Waldemar Iwanek
Journal:  Int J Mol Sci       Date:  2020-10-11       Impact factor: 5.923
  4 in total

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