Affiliation:
1. Centro de Ciências Químicas Farmacêuticas e de Alimentos – CCQFA Universidade Federal de Pelotas – UFPel P. O. box 354 96010-900 Pelotas RS Brazil
2. Departamento de Física Universidade Federal de Santa Maria Av. Roraima, Building 13 97105-900 Santa Maria RS Brazil
3. Departamento de Química Universidade Federal de Santa Maria Av. Roraima, Building 18 97105-340 Santa Maria RS Brazil
Abstract
AbstractHerein, we describe a new method for the synthesis of α‐carbonyl selenocyanates by reacting triselenium dicyanide (TSD) and styrenes under blue light irradiation and O2 atmosphere. The reactions are triggered by the formation of Se‐centered radical species, followed by the addition/oxidation of the styrene π‐bond. α‐Carbonyl selenocyanates and α‐hydroxy selenocyanates were obtained in moderate to excellent yields from aryl‐ and alkyl‐substituted alkenes, respectively. It was demonstrated that α‐carbonyl selenocyanates could be used as a synthetic platform in a multicomponent reaction strategy to prepare 2‐phenylimidazo[1,2‐a]pyridine derivatives, which were evaluated for their photophysical properties. Overall, this new method provides a useful tool for synthesizing α‐carbonyl selenocyanates, and demonstrates their potential for use in the synthesis of other compounds, thus giving new synthetic opportunities to construct organic selenocyanate compounds.
Funder
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul
Financiadora de Estudos e Projetos
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
3 articles.
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