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Synthesis of polyfluorinated benzofurans Full article

Journal Journal of Fluorine Chemistry
ISSN: 0022-1139
Output data Year: 2019, Volume: 227, Article number : UNSP 109371, Pages count : DOI: 10.1016/j.jfluchem.2019.109371
Tags Fluoroheterocycles; o-Iodophenols; Iodination; Cross-coupling; Benzofurans
Authors Politanskaya Larisa 1,2 , Troshkova Nadezhda 1 , Tretyakov Evgeny 1,2 , Xi Chanjuan 3
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Ac Lavrentiev Ave 9, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Pirogova Str 2, Novosibirsk 630090, Russia
3 (Данные Web of science) Tsinghua Univ, Dept Chem, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China

Abstract: A simple and efficient approach to the synthesis of fluorinated benzofurans including the Sonogashira cross-coupling of o-iodophenols with terminal Ph. and n-Bu-acetylenes, followed by intramolecular cyclization, in good to excellent yields is reported.
Cite: Politanskaya L. , Troshkova N. , Tretyakov E. , Xi C.
Synthesis of polyfluorinated benzofurans
Journal of Fluorine Chemistry. 2019. V.227. UNSP 109371 . DOI: 10.1016/j.jfluchem.2019.109371 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Nov 1, 2019
Identifiers:
Web of science: WOS:000497248500005
Scopus: 2-s2.0-85072201182
Elibrary: 41677636
OpenAlex: W2972342482
Citing:
DB Citing
Web of science 7
Scopus 8
Elibrary 9
OpenAlex 7
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