دورية أكاديمية
أعرض في EDS

Decarboxylative ring-opening of 2-oxazolidinones: a facile and modular synthesis of β-chalcogen amines.

التفاصيل البيبلوغرافية
العنوان: Decarboxylative ring-opening of 2-oxazolidinones: a facile and modular synthesis of β-chalcogen amines.
المؤلفون: Galetto FZ; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., da Silva C; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., Beche RIM; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., Balaguez RA; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., Franco MS; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., de Assis FF; Department of Chemistry, Federal University of Santa Catarina Florianópolis SC 88040-900 Brazil galetto.f.z@ufsc.br +554837213649., Frizon TEA; Department of Energy and Sustainability, Federal University of Santa Catarina Araranguá SC Brazil., Su X; Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign Urbana IL 61801 USA.
المصدر: RSC advances [RSC Adv] 2022 Nov 30; Vol. 12 (53), pp. 34496-34502. Date of Electronic Publication: 2022 Nov 30 (Print Publication: 2022).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101581657 Publication Model: eCollection Cited Medium: Internet ISSN: 2046-2069 (Electronic) Linking ISSN: 20462069 NLM ISO Abbreviation: RSC Adv Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Cambridge [England] : Royal Society of Chemistry, [2011]-
مستخلص: 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%.
Competing Interests: There are no conflicts to declare.
(This journal is © The Royal Society of Chemistry.)
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تواريخ الأحداث: Date Created: 20221222 Latest Revision: 20231102
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC9710311
DOI: 10.1039/d2ra06070a
PMID: 36545628
قاعدة البيانات: MEDLINE
الوصف
تدمد:2046-2069
DOI:10.1039/d2ra06070a