A simple and highly efficient procedure for construction of quaternary carbons centers by tributylphosphine catalyzed bis-Michael addition
摘要:
The tributylphosphine-catalyzed bis-Michael addition reaction of various kinds of a,13-unsaturated carbonyl compounds with active methylenes is described. This is a convenient and rapid method for generating quaternary carbons centers and useful procedure for the synthesis of branched core and highly substituted trans cyclohexanones. All the reactions were completed in 60 min and afford the corresponding products in excellent yields. (C) 2013 Elsevier Ltd. All rights reserved.
CuCN catalyzed one pot synthesis of γ-keto diesters: domino double Michael addition followed by Nef reaction
作者:Saleem Farooq、Payare L. Sangwan、Rajeshwar R. Aleti、Praveen K. Chinthakindi、Mushtaq A. Qurishi、Surrinder Koul
DOI:10.1016/j.tetlet.2012.04.071
日期:2012.6
An efficient one pot synthesis of γ-keto diesters through double Michael addition coupled with Nef reaction in the presence of CuCN catalyst and Cs2CO3 base is described. The reaction proceeds rapidly in DCM to give the products in good yields. A plausible mechanism is proposed.
描述了在CuCN催化剂和Cs 2 CO 3碱存在下,通过双迈克尔加成和Nef反应有效地一锅合成γ-酮二酯。该反应在DCM中快速进行,以高收率得到产物。提出了一种合理的机制。