Literature DB >> 16671768

Direct synthesis of bipyrroles using phenyliodine bis(trifluoroacetate) with bromotrimethylsilane.

Toshifumi Dohi1, Koji Morimoto, Akinobu Maruyama, Yasuyuki Kita.   

Abstract

[reaction: see text] The hypervalent iodine(III) reagent, phenyliodine bis(trifluoroacetate) (PIFA), mediates the unprecedented, oxidative coupling reaction of pyrroles to give alpha-linked bipyrroles selectively in the presence of bromotrimethylsilane. This straightforward synthesis could provide 2,3'-bipyrrole by the choice of a N-substituent of pyrrole. Mechanistic consideration of the present reaction is also described.

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Year:  2006        PMID: 16671768     DOI: 10.1021/ol060333m

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


  9 in total

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7.  Facile Synthesis of NH-Free 5-(Hetero)Aryl-Pyrrole-2-Carboxylates by Catalytic C-H Borylation and Suzuki Coupling.

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8.  Synthesis, Structure, and Reactivity of 5-(Aryl)dibenzothiophenium Triflates.

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Review 9.  Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review.

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  9 in total

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