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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2020, том 30, выпуск 1, страницы 34–37 (Mi mendc1092)

Эта публикация цитируется в 3 статьях

2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole in the reactions with terminal acetylenes

A. V. Nemtarevab, I. O. Nasibullinb, R. R. Fayzullina, L. R. Grigor’evab, V. F. Mironovab

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation

Аннотация: 2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole reacts with arylacetylenes or 3-chloropropyne to give 2,7-dichloro-5-methoxy-4-aryl(haloalkyl)-1,2-benzoxaphosphinine 2-oxides. Hydrolysis of the latter leads to the opening of the oxaphosphinine ring and formation of (E)-2-(4-chloro-2-methoxy-6-hydroxyphenyl)ethenylphosphonic acid.

Ключевые слова: dioxaphospholes, phosphoranes, arylacetylenes, cascade reactions, oxaphosphinines, ethenylphosphonic acids.

Язык публикации: английский

DOI: 10.1016/j.mencom.2020.01.011



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