@article{oai:kumadai.repo.nii.ac.jp:00026640,
 author = {一番ヶ瀬, 友紀 and 中島, 誠 and 一番ヶ瀬, 友紀 and Ichibakase, Tomonori and 中島, 誠 and Nakajima, Makoto},
 issue = {20},
 journal = {Synthesis},
 month = {Oct},
 note = {application/pdf, 論文(Article), 1,3-Diol derivatives with three contiguous stereocenters were efficiently prepared by an enantioselective direct aldol–Tishchenko reaction catalyzed by dilithium 3,3’-diphenylbinaphtholate. The reactions of acyclic ketones as aldol donors gave 1,2-syn-1,3-anti diol derivatives, whereas the reactions of cyclic ketones as aldol donors gave 1,2-anti-1,3-anti diol derivatives. Sequential aldol–aldol–Tishchenko reactions gave a triol derivative with five consecutive chiral centers., https://www.thieme-connect.de/DOI/DOI?10.1055/s-0031-1291138},
 pages = {3145--3151},
 title = {Efficient Preparation of 1,3-Diol derivatives with Three Contiguous Stereocenters by an Enantioselective Direct Aldol-Tishchenko Reaction},
 volume = {44},
 year = {2012},
 yomi = {イチバカセ, トモノリ and ナカジマ, マコト}
}