シライ トモヒコ
Shirai Tomohiko
白井 智彦 所属 東邦大学 理学部 化学科 職種 講師 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Rhodium-Catalyzed 1,4-Addition of Lithium 2-Furyltriolborates to Unsaturated Ketones and Esters for Enantioselective Synthesis of gamma-Oxo-Carboxylic Acids By Oxidation of the Furyl Ring with Ozone |
掲載誌名 | 正式名:Chemistry - An Asian Journal ISSNコード:1861-4728 |
出版社 | WILEY-V C H VERLAG GMBH |
巻・号・頁 | 6(3),pp.932-937 |
著者・共著者 | Xiao-Qiang Yu,Tomohiko Shirai,Yasunori Yamamoto,Norio Miyaura |
担当区分 | 2nd著者 |
発行年月 | 2011/03 |
概要 | Rhodium-catalyzed 1,4-addition of lithium 5-methyl-2-furyltriolborate ([ArBACHTUNGTRENUNG(OCH2)(3)CCH3] Li, Ar = 5-methyl-2-furyl) to unsaturated ketones to give beta-furyl ketones was followed by ozonolysis of the furyl ring for enantioselective synthesis of gamma-oxo-carboxylic acids. [RhACHTUNGTRENUNG(nbd)(2)]BF4 (nbd = 2,5-norbornadiene) chelated with 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (binap) or 2,3-bis(diphenylphosphino) butane (chiraphos) gave high yields and high selectivities in a range of 91-99% ee at 30 degrees C in a basic dioxane/water solution. The corresponding reaction of unsaturated esters, such as methyl crotonate, had strong resistance under analogous conditions, but the 1,4-adduct was obtained in 70% yield and with 94% ee when more electron-deficient phenyl crotonate was used as the substrate. |
DOI | 10.1002/asia.201000589 |