@article{oai:chuo-u.repo.nii.ac.jp:00001264,
 author = {小川, 昭弥 and 田中, 宏道 and 秋山, 隆彦 and 福沢, 信一},
 journal = {中央大学理工学研究所論文集},
 month = {Mar},
 note = {application/pdf, Samarium diiodide (SmI2) in the copresence of chlorotrimethylsilane reduces cyclic ketones efficiently, compared with samarium diiodide alone, providing the corresponding reductive coupling products, alcohols, and their silyl ethers with the formation of enol silyl ethers. Possible reaction pathways for this reduction are discussed in detail. In addition, this paper also deals with the reduction of alkyl aryl ketones using a mixed system of metallic samarium and chlorotrimethylsilane, which leads to the pinacol coupling of ketones. The stereoselectivity of this coupling reaction is also investigated., 【査読有】},
 pages = {37--43},
 title = {クロロシラン共存下における低原子価サマリウム試薬によるケトン類の還元反応},
 volume = {7},
 year = {2002},
 yomi = {オガワ, アキヤ and タナカ, ヒロミチ and アキヤマ, タカヒコ and フクザワ, シンイチ}
}