Nouvelles voies d'acces aux 2-ethoxycarbonylallylphosphonates
H Mrabet, H Zantour
Index: Mrabet, Hedi; Zantour, Hedi Phosphorus, Sulfur and Silicon and the Related Elements, 2004 , vol. 179, # 1 p. 25 - 33
Full Text: HTML
Citation Number: 6
Abstract
The Michaelis-Arbusov reaction (method A) and the nucleophilic addition of dialkylphosphites followed by Hoffman olefination (method B) represent two synthetic methods giving a variety of 2-ethoxycarbonylallyl-phosphonates 2, in good yields, from readily accessible ethyl 2-(N, N-dialkylaminomethyl) acrylates 1.
Related Articles:
First synthesis of 2-[alkylamino (diethoxyphosphoryl) methyl] acrylic ethyl esters
[Kraiem, Houda; Abdullah, Meysun Ibrahim; Amri, Hassen Tetrahedron Letters, 2003 , vol. 44, # 3 p. 553 - 555]
[Martinez-Castro, Elisa; Lopez, Oscar; Maya, Ines; Fernandez-Bolanos, Jose G.; Petrini, Marino Green Chemistry, 2010 , vol. 12, # 7 p. 1171 - 1174]
[Cox; Hawkes; Bellini; Ellis; Barrett; Swanborough; Russell; Walker; Barnes; Knee; Lewis; Davies Pesticide Science, 1997 , vol. 50, # 4 p. 297 - 311]