Literature DB >> 12526662

Resorcinarenes as templates: a general strategy for the synthesis of large macrocycles.

Xuehe Li1, Thomas G Upton, Corinne L D Gibb, Bruce C Gibb.   

Abstract

The concept that resorcinarenes can be used as templates for the synthesis of large macrocycles is introduced. By way of example, previously inaccessible, aromatic crown ethers compounds are synthesized.

Entities:  

Year:  2003        PMID： 12526662     DOI： 10.1021/ja029116g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  4 in total

1.  Polyether macrocycles from intramolecular cyclopropanation and ylide formation. Effect of catalyst and coordination.

Authors:  Thomas M Weathers; Yuanhua Wang; Michael P Doyle
Journal:  J Org Chem       Date:  2006-10-13       Impact factor: 4.354

2.  Facile synthesis of symmetrical bis(benzhydryl)ethers using p-toluenesulfonyl chloride under solvent-free conditions.

Authors:  Goutam Brahmachari; Bubun Banerjee
Journal:  Org Med Chem Lett       Date:  2013-02-18

3.  Post-synthetic modification of a macrocyclic receptor via regioselective imidazolium ring-opening.

Authors:  Jia Shang; Brett M Rambo; Xiang Hao; Jun-Feng Xiang; Han-Yuan Gong; Jonathan L Sessler
Journal:  Chem Sci       Date:  2016-03-09       Impact factor: 9.825

Review 4.  From steroids to aqueous supramolecular chemistry: an autobiographical career review.

Authors:  Bruce C Gibb
Journal:  Beilstein J Org Chem       Date:  2016-04-12       Impact factor: 2.883
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.