New Morita-Baylis-Hillman (MBH) phosphonium salts from alcohols to the synthesis of 2-alkenyl- and 2-alkylidenecyclohexenones

被引:0
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作者
Elleuch H. [1 ]
Msalbi D. [2 ]
Mhasni O. [5 ]
Yaccoubi F. [1 ,4 ]
Aifa S. [2 ]
Legros J. [3 ]
Rezgui F. [1 ]
机构
[1] Université de Tunis El Manar, Faculté des Sciences de Tunis, Laboratoire de Chimie Organique Structurale LR99ES14, Campus Universitaire, Tunis
[2] Université de Sfax, Laboratoire de Procédés de Criblage Moléculaire et Cellulaire, Centre de Biotechnologie de Sfax
[3] Laboratory COBRA University of Rouen Normandy 1, rue Lucien Tesnière, Mont-Saint-Aignan
[4] Department of Chemistry, Faculty of Science and Humanity Studies at Al Quwayiyah, Shaqra University, Al-Quwayiyah
[5] Laboratory of Materials, Treatement and Analysis LMTA, LR 15 INRAP 03, Institute National for Research and Physico-Chemical Analysis (INRAP), Biotechpole Sidi Thabet 2020, Tunis
关键词
1,3-diene; 2-alkenylcyclohexenones; 2-alkylidenecyclohexenones; Phosphonium salt; Wittig olefination; Wittig reaction;
D O I
10.1016/j.molstruc.2023.135532
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摘要
Most of synthetic methods for 2- and 3-cyclohexenone derivatives start from limited substrates and therefore their efficiency still limited. In this paper, we report a general synthetic approach for such derivatives using MBH adducts, as substrates easily synthesized under standard conditions. For this purpose, a one-pot conversion of MBH alcohols into the corresponding phosphonium salts is carried out in high yields using PPh3 and an aqueous solution of HBr (48%), both at room temperature. Following purification and characterization of the title products, their further treatment at room temperature with either RCHO/tBuOK or only tBuOK, as the base, yields the corresponding 2-alkenyl- and 2-alkylidenecyclohexenones in good yields through Wittig olefinations or δ-elimination reactions of PPh3.HBr. © 2023 Elsevier B.V.
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