Synthesis of Optically Active Organofluorides by Ring Opening of Oxazolidinone-Fused Aziridines

التفاصيل البيبلوغرافية
العنوان: Synthesis of Optically Active Organofluorides by Ring Opening of Oxazolidinone-Fused Aziridines
المؤلفون: Hung-Che Chen, Chi-Yun Liu, Venkatachalam Angamuthu, Wei-Chen Chen, Chi-Sheng Wen, Duen-Ren Hou
المصدر: Organic Letters. 25:190-194
بيانات النشر: American Chemical Society (ACS), 2022.
سنة النشر: 2022
مصطلحات موضوعية: Organic Chemistry, Physical and Theoretical Chemistry, Biochemistry
الوصف: A general method for synthesizing optically active, primary, secondary, and tertiary organofluorides was developed. This chiral pool synthesis utilized the skeleton of arabinose to generate diastereomerically pure 2-oxazolidinone-fused aziridines, which underwent ring opening with a fluoride anion. The adducts, polyoxygenated organofluorides, were useful precursors to various fluorinated compounds, such as fluorinated amino acids.
تدمد: 1523-7052
1523-7060
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d6696159387d805d885f6710939c328
https://doi.org/10.1021/acs.orglett.2c04042
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....0d6696159387d805d885f6710939c328
قاعدة البيانات: OpenAIRE