Functionalized organolithium reagents. 8. Novel (. alpha.,. beta.-epoxyalkyl) lithium reagents via the lithiation of organyl-substituted epoxides
JJ Eisch, JE Galle
Index: Eisch, John J.; Galle, James E. Journal of Organic Chemistry, 1990 , vol. 55, # 16 p. 4835 - 4840
Full Text: HTML
Citation Number: 64
Abstract
Results Organyl-Substituted Epoxides. In order to investigate the acidifying character of various organic groups CY to the epoxide linkages (R" in eq 2), the compounds depicted in Scheme I were subjected to the action of the 1: l complex of tert-butyllithium and TMEDA at temperatures of-80 to-115 OC.' After a suitable interval the reaction
Related Articles:
[Walling, Cheves; El-Taliawi, Gamil M.; Amarnath, Kalyani Journal of the American Chemical Society, 1984 , vol. 106, p. 7573 - 7578]
[Walling, Cheves; El-Taliawi, Gamil M.; Amarnath, Kalyani Journal of the American Chemical Society, 1984 , vol. 106, p. 7573 - 7578]
[Chen, Victor X.; Boyer, Francois-Didier; Rameau, Catherine; Pillot, Jean-Paul; Vors, Jean-Pierre; Beau, Jean-Marie Chemistry - A European Journal, 2013 , vol. 19, # 15 p. 4849 - 4857]
[Saedi, Zahra; Tangestaninejad, Shaharm; Moghadam, Majid; Mirkhani, Valiollah; Mohammadpoor-Baltork, Iraj Journal of Coordination Chemistry, 2012 , vol. 65, # 3 p. 463 - 473]
Tautomerism of the monohydroxy derivatives of five-membered oxygen, nitrogen and sulfur heterocycles
[Capon, Brian; Kwok, Fu-Chiu Journal of the American Chemical Society, 1989 , vol. 111, # 14 p. 5346 - 5356]