ChemInform Abstract: ICI-Mediated Intramolecular Twofold Iodoarylation of Diynes and Diynyl Diethers and Amines: Synthesis of Bis(2H-hydronaphthalene and chromene) and 2H-Quinoline Bearing an Alkenyl Iodide Moiety

ChemInform Abstract: ICI-Mediated Intramolecular Twofold Iodoarylation of Diynes and Diynyl Diethers and Amines: Synthesis of Bis(2H-hydronaphthalene and chromene) and 2H-Quinoline Bearing an Alkenyl Iodide Moiety

The reaction can be applied to a broad range of diynes under mild conditions with good to high yields.

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Veröffentlicht in:ChemInform 2014-04, Vol.45 (17), p.no-no
Hauptverfasser: Mo, Juntae, Choi, Wonseok, Min, Jiae, Kim, Cheol-Eui, Eom, Dahan, Kim, Sung Hong, Lee, Phil Ho
Format: Artikel
Sprache:eng
Schlagworte:
benzopyran derivatives
C-C bond formation
quinoline derivatives
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container_issue 17
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container_title ChemInform
container_volume 45
creator Mo, Juntae
Choi, Wonseok
Min, Jiae
Kim, Cheol-Eui
Eom, Dahan
Kim, Sung Hong
Lee, Phil Ho
description The reaction can be applied to a broad range of diynes under mild conditions with good to high yields.
doi_str_mv 10.1002/chin.201417148
format Article
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source Wiley Online Library Journals
subjects benzopyran derivatives
C-C bond formation
quinoline derivatives
title ChemInform Abstract: ICI-Mediated Intramolecular Twofold Iodoarylation of Diynes and Diynyl Diethers and Amines: Synthesis of Bis(2H-hydronaphthalene and chromene) and 2H-Quinoline Bearing an Alkenyl Iodide Moiety
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