Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Darya Syniuchenko"'
Autor:
Dmitriy M. Volochnyuk, Andrii Khutorianskyi, Anastasiia O. Osipova, Konstantin S. Gavrilenko, Igor V. Komarov, Bohdan V. Vashchenko, Anton Tsymbaliuk, Bohdan A. Chalyk, Kyrylo Danyleiko, Andriy V. Kozytskiy, Oleksandr O. Grygorenko, Anastasiia Grynyova, Darya Syniuchenko, Angelina V. Biitseva
Publikováno v:
The Journal of Organic Chemistry. 87:1001-1018
An efficient synthesis (up to a 200 g scale) of 3-hydroxypyrrolidin-2-ones bearing alkyl substituents or functional groups at the C-5 position is described. The reaction sequence started from 1,3-dipolar cycloaddition of in situ generated nitrile oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e0dfe45835f1cddbf413017be7d0a05
https://doi.org/10.1021/acs.joc.1c02301
https://doi.org/10.1021/acs.joc.1c02301
Autor:
Bohdan A, Chalyk, Andrii V, Khutorianskyi, Bohdan V, Vashchenko, Kyrylo, Danyleiko, Anastasiia, Grynyova, Anastasiia O, Osipova, Andriy, Kozytskiy, Darya, Syniuchenko, Anton, Tsymbaliuk, Konstantin S, Gavrilenko, Angelina V, Biitseva, Dmitriy M, Volochnyuk, Igor V, Komarov, Oleksandr O, Grygorenko
Publikováno v:
The Journal of organic chemistry. 87(2)
An efficient synthesis (up to a 200 g scale) of 3-hydroxypyrrolidin-2-ones bearing alkyl substituents or functional groups at the C-5 position is described. The reaction sequence started from 1,3-dipolar cycloaddition of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2dfeda69f122f908cbb0b77cccccd23
https://pubmed.ncbi.nlm.nih.gov/34843235
https://pubmed.ncbi.nlm.nih.gov/34843235