Literature DB >> 17685536

Triptycenediols by rhodium-catalyzed [2+2+2] cycloaddition.

Mark S Taylor1, Timothy M Swager.   

Abstract

An efficient, modular synthesis of triptycene derivatives is presented, in which the triptycene ring system is constructed from readily available anthraquinone and alkyne starting materials. A rhodium-catalyzed alkyne cyclotrimerization reaction serves as the key step in this new method for the preparation of these useful unnatural products.

Entities:  

Year:  2007        PMID: 17685536     DOI: 10.1021/ol701642j

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


  3 in total

1.  Triptycene diols: a strategy for synthesizing planar π systems through catalytic conversion of a poly(p-phenylene ethynylene) into a poly(p-phenylene vinylene).

Authors:  Brett VanVeller; Dale Robinson; Timothy M Swager
Journal:  Angew Chem Int Ed Engl       Date:  2011-12-23       Impact factor: 15.336

2.  Polycyclic aromatic triptycenes: oxygen substitution cyclization strategies.

Authors:  Brett VanVeller; Derek J Schipper; Timothy M Swager
Journal:  J Am Chem Soc       Date:  2012-04-18       Impact factor: 15.419

Review 3.  Triptycene Derivatives: From Their Synthesis to Their Unique Properties.

Authors:  Mateusz Woźny; Adam Mames; Tomasz Ratajczyk
Journal:  Molecules       Date:  2021-12-31       Impact factor: 4.411

  3 in total

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