Gold(I)-catalyzed 6-endo hydroxycyclization of 7-substituted-1,6-enynes
Autor: | Sanjuán Cortázar, Ana María, Martínez Cuezva, Alberto, García García, Patricia, Fernández Rodríguez, Manuel A., Sanz Díez, Roberto |
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Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: | |
Zdroj: | Repositorio Institucional de la Universidad de Burgos (RIUBU) instname |
Popis: | The cyclization of o-(alkynyl)-3-(methylbut-2-enyl)benzenes, 1,6-enynes having a condensed aromatic ring at C3–C4 positions, has been studied under the catalysis of cationic gold(I) complexes. The selective 6-endo-dig mode of cyclization observed for the 7-substituted substrates in the presence of water or methanol giving rise to hydroxy(methoxy)-functionalized dihydronaphthalene derivatives is highly remarkable in the context of the observed reaction pathways for the cycloisomerizations of 1,6-enynes bearing a trisubstituted olefin Ministerio de Ciencia e Innovación (MICINN) and FEDER (CTQ2010-15358) |
Databáze: | OpenAIRE |
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