Silico-alkylation of Sodio Esters with Trimethyl-chlorosilane to Form Silyl Esters1
CR Hance, CR Hauser
Index: Hance; Hauser Journal of the American Chemical Society, 1953 , vol. 75, p. 994
Full Text: HTML
Citation Number: 17
Abstract
These reactions are assumed to produce the C-derivatives, I and 11, rather than the 0- derivative, for example, 111. The related reaction of sodioacetoacetic ester with triethylchlorosilane has been assumed to form such an 0-derivative (IV) 4 but this structure has been questioned. 6
Related Articles:
[Albaugh-Robertson, Pamela; Katzenellenbogen, John A. Journal of Organic Chemistry, 1983 , vol. 48, # 26 p. 5288 - 5302]
[Harada, Toshiro; Egusa, Takayuki; Igarashi, Yasuto; Kinugasa, Motoharu; Oku, Akira Journal of Organic Chemistry, 2002 , vol. 67, # 20 p. 7080 - 7090]
[Emde, Herbert; Simchen, Gerhard Liebigs Annalen der Chemie, 1983 , # 5 p. 816 - 834]
[Schmidt,U.; Schwochau,M. Tetrahedron Letters, 1967 , p. 875 - 879]
Preparation and reactivity of persistent and stable silyl-substituted bisketenes
[Zhao, Da-Chuan; Allen, Annette D.; Tidwell, Thomas T. Journal of the American Chemical Society, 1993 , vol. 115, # 22 p. 10097 - 10103]