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Stereoselective synthesis of trans olefins by the reaction of Wittig reagents with selenium. Formation of selenocarbonyl compounds. |
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| Authors: | Kentaro Okuma Jun-ichi Sakata Yuji Tachibana Takumi Honda Hiroshi Ohta |
| Institution: | Department of Chemistry, Faculty of Science, Fukuoka University, Jonan-ku, Fukuoka 814-01, Japan |
| Abstract: | Wittig reagents were successfully changed to symmetrical olefins when treated with elemental selenium. The reaction proceeds through a selenocarbonyl intermediate, which existence was confirmed by Diels-Alder reaction. |
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