Literature DB >> 15876011

Facile syntheses of quater-, penta-, and sexipyrroles.

Jonathan L Sessler1, Apolonio Aguilar, David Sanchez-Garcia, Daniel Seidel, Thomas Köhler, Forrest Arp, Vincent M Lynch.   

Abstract

alpha,alpha-Linked oligopyrroles are attractive precursors for both expanded porphyrin and conducting polymer chemistry. We demonstrate facile methods for synthesizing quater-, penta-, and sexipyrroles from more readily available bi- and terpyrrole intermediates. These products demonstrate stability in their brightly colored oxidized forms, while reduction using borohydride reagents gives the corresponding all-pyrrole oligomers, which oxidize readily in air. The oxidized quater- and sexipyrroles were characterized by single-crystal X-ray diffraction analysis.

Entities:  

Year:  2005        PMID: 15876011     DOI: 10.1021/ol050151c

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


  2 in total

1.  Gram-Scale Synthesis of a Bench-Stable 5,5″-Unsubstituted Terpyrrole.

Authors:  James T Brewster; Hadiqa Zafar; Matthew McVeigh; Christopher D Wight; Gonzalo Anguera; Axel Steinbrück; Vincent M Lynch; Jonathan L Sessler
Journal:  J Org Chem       Date:  2018-07-03       Impact factor: 4.354

2.  Pyrrole N-H Anion Complexes.

Authors:  Gabriela I Vargas-Zúñiga; Jonathan L Sessler
Journal:  Coord Chem Rev       Date:  2017-04-20       Impact factor: 22.315

  2 in total

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