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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2021, том 31, выпуск 5, страницы 654–656 (Mi mendc1012)

Эта публикация цитируется в 4 статьях

Communications

Synthesis of vicinal (alkylamino)alkynylcyclopropanes from geminal alkynyl(chloro)cyclopropanes

V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: New N-Boc-alkyl(2-alkynylcyclopropyl)amines were synthesized from 1-alkynyl-1-chlorocyclopropanes and N-Boc- alkylamines under the action of ButOK in DMSO, the intermediates having been the corresponding conjugated alkynylcyclopropenes. The Boc-derivatives can be converted into free secondary 2-alkynylcyclopropylamines, as well as β-lithiated with subsequent alkylation.

Ключевые слова: alkynyl(chloro)cyclopropanes, 1-amino-2-alkynylcyclopropanes, cyclopropylamines, cyclopropenes, protecting groups, directing groups, lithiation, alkylation, stereoselectivity.

Язык публикации: английский

DOI: 10.1016/j.mencom.2021.09.020



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