Literature DB >> 11009381

Convenient iterative synthesis of an octameric tetracarboxylate-functionalized oligophenylene rod with divergent end groups

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Abstract

Oligo(p-phenylene) rigid rod 10 is synthesized via a functional group-tolerant molecular doubling approach. Preparative chromatographic methods, protecting groups, boronic acid isolations, and Grignard or organolithium reagents are not used. The convenient synthesis of well-defined, polar-functionalized oligophenylene rigid rods could afford ready access to a variety of useful electronic organic materials.

Entities:  

Year:  2000        PMID: 11009381     DOI: 10.1021/ol000204k

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


  4 in total

1.  Rhodamine analogues for molecular ruler applications.

Authors:  Yu-Hsuan Chu; Jorge O Escobedo; Meiyan Jiang; Peter S Steyger; Robert M Strongin
Journal:  Dyes Pigm       Date:  2016-03-01       Impact factor: 4.889

2.  Live cell imaging of a fluorescent gentamicin conjugate.

Authors:  Jorge O Escobedo; Yu-Hsuan Chu; Qi Wang; Peter S Steyger; Robert M Strongin
Journal:  Nat Prod Commun       Date:  2012-03       Impact factor: 0.986

3.  Progress toward red and near-infrared (NIR) emitting saccharide sensors.

Authors:  Martha Sibrian-Vazquez; Jorge O Escobedo; Mark Lowry; Robert M Strongin
Journal:  Pure Appl Chem       Date:  2012-04-29       Impact factor: 2.453

4.  Iterative Exponential Growth of Oxygen-Linked Aromatic Polymers Driven by Nucleophilic Aromatic Substitution Reactions.

Authors:  Tyler J Jaynes; Mona Sharafi; Joseph P Campbell; Jessica Bocanegra; Kyle T McKay; Kassondra Little; Reilly Osadchey Brown; Danielle L Gray; Toby J Woods; Jianing Li; Severin T Schneebeli
Journal:  Front Chem       Date:  2021-04-28       Impact factor: 5.545

  4 in total

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