Tetrahedron Letters p. 5147 - 5150 (1984)
Update date:2022-08-03
Topics:
Okazaki, Renji
Ishii, Akihiko
Inamoto, Naoki
The title reaction afforded selenophilic, carbophilic, and reduction products depending on the kinds of the organometallic reagents and the heterophilic nature of the reaction was more conspicuous in the reaction with the selenoketone than with the corres
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(2003)Doi:10.1039/c9nj02829c
(2019)Doi:10.1039/b005269h
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(1984)Doi:10.1016/j.tet.2007.07.108
(2007)
