2026-08-20T03:28:09Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/104992025-05-28T00:05:20Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594

Martínez Núñez, Clara Velasco Pérez, Noelia Sanz Díez, Roberto Suárez Pantiga, Samuel 2025-05-27T11:09:10Z 2025-05-27T11:09:10Z 2024-01 1359-7345 http://hdl.handle.net/10259/10499 10.1039/D3CC06194A 1364-548X Conjugated 1-bromo or 1-iodo-1,3-dienes bearing a sulfide substituent have been synthesized via 1,2-sulfur migration from propargylic thioethers upon activation with NIS or NBS. The reaction generally proceeds with high control over the regio- and diastereoselectivity. Highly substituted thiophenes and selenophenes are easily obtained from the generated dienes. We gratefully acknowledge MCIN (PID2020-115789GB-C21/ AEI/10.13039/501100011033), and Junta de Castilla y Leo ´n and FEDER (BU028P23) for financial support. C. M.-N. thanks Junta de Castilla y Leo´n and Fondo Social Europeo, for a predoctoral contract. S. S.-P. thanks a Ramo ´n y Cajal (RYC2021-031533-I) contract by MCIN/AEI/10.13039/501100011033 and European Union ‘‘NextGenerationEU’’/PRTR. application/pdf eng Royal Society of Chemistry Chemical Communications. 2024, V. 60, n. 13, p. 1794-1797 https://doi.org/10.1039/D3CC06194A Atribución 4.0 Internacional http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess Química Química orgánica Chemistry Chemistry, Organic Synthesis of highly substituted 1,3-dienes through halonium promoted 1,2-sulfur migration of propargylic thioethers info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Chemical Communications 60 13 1794 1797