Academic Journal

Thiocarbamoyl Fluoride Synthesis by Deconstructive Diversification of Arylated Tetrahydroisoquinolines

التفاصيل البيبلوغرافية
العنوان: Thiocarbamoyl Fluoride Synthesis by Deconstructive Diversification of Arylated Tetrahydroisoquinolines
المؤلفون: Wentao Xu (187610), Fang Liu (13271), Jiajun Li (1410187), Muzi Li (698159), Jin Xie (690890), Chengjian Zhu (1492816)
سنة النشر: 2021
المجموعة: Smithsonian Institution: Digital Repository
مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Molecular Biology, Biotechnology, Evolutionary Biology, Ecology, Developmental Biology, Marine Biology, Chemical Sciences not elsewhere classified, thiocarbamoyl fluorides, Thiocarbamoyl Fluoride Synthesis, access, amines, Arylated Tetrahydroisoquinolines De.
الوصف: Deconstructive functionalization of cyclic amines can provide access to chemicals with diverse skeletons. We report the conversion of tertiary amines to thiocarbamoyl fluorides, a reaction enabled by photoredox catalysis and tolerating different functional groups while avoiding strong oxidants. A one-pot synthetic method from tertiary amines and AgF has been developed to get access to trifluoromethylamines. The synthesized thiocarbamoyl fluorides can be further transferred into esters.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
Relation: https://figshare.com/articles/journal_contribution/Thiocarbamoyl_Fluoride_Synthesis_by_Deconstructive_Diversification_of_Arylated_Tetrahydroisoquinolines/15078893
DOI: 10.1021/acs.joc.1c01468.s001
الاتاحة: https://doi.org/10.1021/acs.joc.1c01468.s001
Rights: CC BY-NC 4.0
رقم الانضمام: edsbas.CF64E255
قاعدة البيانات: BASE