Chemistry–A European Journal

New and Facile Approach for the Synthesis of (E)?螃?, β??Unsaturated Esters and Ketones

B China Raju, P Suman

Index: China Raju, Bhimapaka; Suman, Pathi Chemistry - A European Journal, 2010 , vol. 16, # 39 p. 11840 - 11842

Full Text: HTML

Citation Number: 25

Abstract

Preparation of (E)-α, β-unsaturated esters and ketones is an important task in organic synthesis.[1] Such esters and ketones are excellent building blocks for the synthesis of a plethora of synthetic and natural products.[2] The most versatile and widely used methods are the Wittig reaction [3] with aldehydes by using alkoxycarbonylmethylene (triphenyl) phosphoranes and the Horner–Wadsworth–Emmons [4] procedure using trialkyl ...

Related Articles:

“Nok”: A Phytosterol-Based Amphiphile Enabling Transition-Metal-Catalyzed Couplings in Water at Room Temperature

[Wang, Peng; Liu, Chun-Rong; Sun, Xiu-Li; Chen, Shuai-Shuai; Li, Jun-Fang; Xie, Zuowei; Tang, Yong Chemical Communications, 2012 , vol. 48, # 2 p. 290 - 292]

Heck–Matsuda reaction of arenediazonium salts in water

[Salabert, Jordi; Sebastian, Rosa Maria; Vallribera, Adelina; Civicos, Jose Francisco; Najera, Carmen Tetrahedron, 2013 , vol. 69, # 12 p. 2655 - 2659]

Nucleophilic carbene-catalyzed redox-esterification reaction of α-halo-α, β-unsaturated aldehyde

[Wang, Xiang-Bo; Zou, Xiao-Lei; Du, Guang-Fen; Liu, Zhi-Yong; Dai, Bin Tetrahedron, 2012 , vol. 68, # 32 p. 6498 - 6503]

Pd (OAc) 2-catalyzed Oxidative coupling reaction of benzenes with olefins in the presence of molybdovanadophosphoric acid under atmospheric dioxygen and air

[Journal of Organic Chemistry, , vol. 69, # 4 p. 1221 - 1226]

An efficient and general method for the Heck and Buchwald–Hartwig coupling reactions of aryl chlorides

[Lee, Dong-Hwan; Taher, Abu; Hossain, Shahin; Jin, Myung-Jong Organic Letters, 2011 , vol. 13, # 20 p. 5540 - 5543]

More Articles...