@article{oai:kumadai.repo.nii.ac.jp:00024784,
 author = {上田, 知弘 and Ueda, Tomohiro and 一番ヶ瀬, 友紀 and Ichibakase, Tomonori and 折戸, 裕哉 and Orito, Yuya and 中島, 誠 and Nakajima, Makoto and 上田, 知弘 and Ueda, Tomohiro and Tanaka, Kana and 一番ヶ瀬, 友紀 and Ichibakase, Tomonori and 折戸, 裕哉 and Orito, Yuya and 中島, 誠 and Nakajima, Makoto},
 issue = {39},
 journal = {Tetrahedron},
 month = {Sep},
 note = {application/pdf, 論文(Article), Enantioselective alkynylation of aldehydes and ketones was accomplished using trimethoxysilylalkynes as alkynylating reagents and lithium 3,3′-diphenylbinaphtholate as a catalyst. Optically active propargylic alcohols were obtained in good to high chemical yields and enantioselectivities. Alkynylation of acetylpyridines afforded biologically active pyridyl propargylic alcohols in good enantioselectivities., http://www.sciencedirect.com/science/article/pii/S0040402010011555},
 pages = {7726--7731},
 title = {Enantioselective alkynylation of carbonyl compounds with trimethoxysilylalkynes catalyzed by lithium binaphtholate},
 volume = {66},
 year = {2010},
 yomi = {ウエダ, トモヒロ and イチバカセ, トモノリ and オリト, ユウヤ and ナカジマ, マコト and ウエダ, トモヒロ and イチバカセ, トモノリ and オリト, ユウヤ and ナカジマ, マコト}
}