翻訳と辞書 |
Barton-Zard synthesis : ウィキペディア英語版 | Barton–Zard reaction The Barton-Zard reaction is a route to pyrrole derivatives via the reaction of a nitroalkene with an α-isocyanoacetate under basic conditions.〔 pp.43-4〕 It is named after Derek Barton and Samir Zard who first reported it in 1985. ==Mechanism== The mechanism consists of five steps: * Base catalyzed carbonyl enolizaton of the α-isocyanide. * Michael-type addition between the α-isocyanide carbonyl enolate and the nitroalkene. * 5-endo-dig cyclization (see: Baldwin's rules). * Base catalyzed elimination of the nitro group. * 1,5-sigmatropic rearrangement leading to aromatisation.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Barton–Zard reaction」の詳細全文を読む
スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース |
Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.
|
|