Literature DB >> 12170799

A facile synthesis of novel types of cyclodextrin derivatives by insertion of an aromatic dicarbonyl spacer into a permethylated alpha-cyclodextrin skeleton.

Toshiyuki Kida1, Takao Michinobu, Wanbin Zhang, Yohji Nakatsuji, Isao Ikeda.   

Abstract

Novel types of cyclodextrin derivatives are easily synthesized by the insertion of an aromatic dicarbonyl spacer into the skeleton of permethylated alpha-cyclodextrin, and the isophthaloyl-inserted one shows almost the same complexing ability toward p-nitrophenol as permethylated beta-cyclodextrin.

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Year:  2002        PMID: 12170799     DOI: 10.1039/b204960k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Selective modifications at the different positions of cyclodextrins: a review of strategies.

Authors:  Jia Yue Liu; Xiao Zhang; Bing Ren Tian
Journal:  Turk J Chem       Date:  2020-04-01       Impact factor: 1.239

2.  One-Pot Synthesis of Asymmetrically Difunctionalized Oligomaltosides by Cyclodextrin Ring Opening.

Authors:  Matthieu Pélingre; Meriem Smadhi; Abed Bil; Véronique Bonnet; José Kovensky
Journal:  ChemistryOpen       Date:  2021-04       Impact factor: 2.911

  2 in total

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