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Título
Alkynylthioimidazolium Salts: Efficient Reagents for the Synthesis of Alkynyl Sulfides by Electrophilic Thioalkynylation
Autor(es)
Palabras clave
Alkynylthioimidazolium Salts
Alkynyl Sulfides
Electrophilic Thioalkynylation
alkynyl selenides
hypervalent
Fecha de publicación
2016
Editor
Wiley
Citación
J. Peña, G. Talavera, B. Waldecker, M. Alcarazo, Chem. Eur. J. 2017, 23, 75.
Resumen
[EN]The efficient synthesis of a series of alkynylthioimidazolium salts through reaction of organozinc compounds with dibromo(imidazolium)sulfuranes is reported. Addition of Grignard reagents to these new species provided a highly modular, clean, and scalable access to a broad variety of alkynyl sulfides in good-to-excellent yields. The utility of this protocol was showcased by the preparation of alkynyl sulfides, which are particularly difficult to obtain or simply unavailable through the existing methodologies. In addition, the synthetic method was extended to the preparation of alkynyl selenides.
URI
ISSN
0947-6539
DOI
10.1002/chem.201604760
Versión del editor
Aparece en las colecciones
- DQANB. Artículos [108]
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