Literature DB >> 30276393

An alternative route for the synthesis of hydroxylated pillar[5]arene-based amphiphiles.

Talal F Al-Azemi1, Mickey Vinodh, Fatemeh H Alipour, Abdirahman A Mohamod.   

Abstract

Conformational mobilities of the units and host-guest complexation with n-octyltrimethylammonium hexafluorophosphate of the synthesized perbenzylated pillar[5]arenes were studied. The formed complex was confirmed by proton nuclear magnetic resonance spectroscopy and mass spectral analysis. Hydroxylated pillar[5]arene-based amphiphiles were synthesized by a co-cyclization strategy followed by catalytic hydrogenation. This approach unlocks the synthesis and the design of a wide range of structural manipulations to these amphiphilic pillararenes.

Entities:  

Year:  2018        PMID: 30276393     DOI: 10.1039/c8ob02074d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Constitutional isomers of brominated-functionalized copillar[5]arenes: synthesis, characterization, and crystal structures.

Authors:  Talal F Al-Azemi; Mickey Vinodh; Fatemeh H Alipour; Abdirahman A Mohamod
Journal:  RSC Adv       Date:  2019-05-03       Impact factor: 4.036

2.  Synthesis, functionalization, and isolation of planar-chiral pillar[5]arenes with bulky substituents using a chiral derivatization agent.

Authors:  Talal F Al-Azemi; Mickey Vinodh; Fatemeh H Alipour; Abdirahman A Mohamod
Journal:  RSC Adv       Date:  2019-07-26       Impact factor: 4.036

  2 in total

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