Cargando…

Hydromethylation of Unactivated Olefins

[Image: see text] A solution to the classic unsolved problem of olefin hydromethylation is presented. This highly chemoselective method can tolerate labile and reactive chemical functionalities and uses a simple set of reagents. An array of olefins, including mono-, di-, and trisubstituted olefins,...

Descripción completa

Detalles Bibliográficos
Autores principales: Dao, Hai T., Li, Chao, Michaudel, Quentin, Maxwell, Brad D., Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490774/
https://www.ncbi.nlm.nih.gov/pubmed/26088401
http://dx.doi.org/10.1021/jacs.5b05144
Descripción
Sumario:[Image: see text] A solution to the classic unsolved problem of olefin hydromethylation is presented. This highly chemoselective method can tolerate labile and reactive chemical functionalities and uses a simple set of reagents. An array of olefins, including mono-, di-, and trisubstituted olefins, are all smoothly hydromethylated. This mild protocol can be used to simplify the synthesis of a specific target or to directly “edit” complex natural products and other advanced materials. The method is also amenable to the simple installation of radioactive and stable labeled methyl groups.