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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2018, том 28, выпуск 1, страницы 61–63 (Mi mendc1664)

Эта публикация цитируется в 21 статьях

Communications

Effective stereoselective approach to substituted 1,4-dioxane-2,5-diones as prospective substrates for ring-opening polymerization

B. A. Lozhkina, A. V. Shlyakhtina, V. V. Bagrova, P. V. Ivchenkoab, I. E. Nifant'evab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: Intramolecular cyclization of α-bromoacyl derivatives of α-hydroxy acids affords 1,4-dioxane-2,5-diones. The method is suitable to obtain mono- and disubstituted products, the latter being formed stereoselectively as (S,S)-diastereomers, as confirmed by DFT modeling.

Язык публикации: английский

DOI: 10.1016/j.mencom.2018.01.020



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