Bulletin of the Chemical Society of Japan p. 197 - 206 (1997)
Update date:2022-08-02
Topics:
Shimada, Kazuaki
Jin, Norikazu
Kawaguchi, Michiko
Dobashi, Kumiko
Nagano, Yumi
Fujimura, Manabu
Kudoh, Eiichi
Kai, Tomonari
Saito, Noboru
Masuda, Jun-Ichi
Iwaya, Masaki
Fujisawa, Hiroyuki
Aoyagi, Shigenobu
Takikawa, Yuji
Selenoaldehydes and selenoketones were generated in situ, by treating aldehydes or ketones, respectively, with bis(1,5-cyclooctanediylboryl) selenide; the resulting selenocarbonyl compounds were trapped with 2,3-dimethyl-1,3-butadiene to give the correspo
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Doi:10.1016/S0040-4039(99)00518-3
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(1999)Doi:10.1039/b006916g
(2001)Doi:10.1021/jm101593u
(2011)Doi:10.1007/BF00904523
(1972)Doi:10.1016/S0040-4020(99)00128-3
(1999)
