Hemisynthesis of methyl pyrethroates from γ-alkoxy-alkylidene malonates and isopropylidenediphenylsulfurane and isopropylidenetriphenylphosphorane
A Krief, A Froidbise
Index: Krief, Alain; Froidbise, Alexandre Tetrahedron, 2004 , vol. 60, # 35 p. 7637 - 7658
Full Text: HTML
Citation Number: 19
Abstract
Hemisynthesis of methyl pyrethroates from γ-alkoxy-alkylidene malonates and isopropylidenediphenylsulfurane and isopropylidenetriphenylphosphorane is disclosed. It takes advantage of the high degree of stereocontrol observed in the cyclopropanation of γ- alkoxy-alkylidene malonates by the above mentioned ylides.
Related Articles:
[Karmee, Sanjib Kumar Synthetic Communications, 2013 , vol. 43, # 3 p. 450 - 455,6]
[Procopio, Antonio; Dalpozzo, Renato; De Nino, Antonio; Maiuolo, Loredana; Nardi, Monica; Russo, Beatrice Advanced Synthesis and Catalysis, 2005 , vol. 347, # 10 p. 1447 - 1450]
[Shaikh, Nadim S.; Junge, Kathrin; Beller, Matthias Organic Letters, 2007 , vol. 9, # 26 p. 5429 - 5432]
[Matsumoto, Yoshihiko; Mita, Keisuke; Hashimoto, Keiji; Iio, Hideo; Tokoroyama, Takashi Tetrahedron, 1996 , vol. 52, # 28 p. 9387 - 9398]
[Malik, Satish; Kartha, K. P. Ravindranathan Synlett, 2009 , # 11 p. 1809 - 1811]