@article{268b162abf83485ca690fff28a27c1fd,
title = "Decarboxylative ring-opening of 2-oxazolidinones: a facile and modular synthesis of β-chalcogen amines",
abstract = "We report herein the synthesis of primary and secondary β-chalcogen amines through the regioselective ring-opening reaction of non-activated 2-oxazolidinones promoted by in situ generated chalcogenolate anions. The developed one-step protocol enabled the preparation of β-selenoamines, β-telluroamines and β-thioamines with appreciable structural diversity and in yields of up to 95%.",
author = "Galetto, {F{\'a}bio Z.} and {da Silva}, Cleiton and Beche, {Ricardo I.M.} and Balaguez, {Renata A.} and Franco, {Marcelo S.} and {de Assis}, {Francisco F.} and Frizon, {Tiago E.A.} and Xiao Su",
note = "Funding Information: The authors gratefully acknowledge FAPESC, CAPES and CNPq (grant 457479/2014-0) for financial support. X. Su acknowledges support by the National Science Foundation (NSF) under CBET Grant # 1942971. We also express our gratitude to Ajinomoto do Brasil for the kind donation of amino acids. Finally, we thank CEBIME-UFSC for the HRMS analyzes. Publisher Copyright: {\textcopyright} 2022 The Royal Society of Chemistry.",
year = "2022",
month = nov,
day = "30",
doi = "10.1039/D2RA06070A",
language = "English (US)",
volume = "12",
pages = "34496--34502",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "53",
}