Journal of Heterocyclic Chemistry

Differing reactivities and products in the reaction of some N??methylimidazol??2??yl, oxazol??2??yl??and thiazol??2??ylsilanes and??stannanes with acid chlorides

P Jutzi, U Gilge

Index: Jutzi, Peter; Gilge, Ullrich Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 1011 - 1014

Full Text: HTML

Citation Number: 14

Abstract

Abstract Some new N-methylimidazoles, oxazoles and thiazoles (compounds 7-15) with a keto-function in the 2-position have been synthesized by the reaction of heterocyclic substituted silanes and stannanes with the corresponding acid chlorides. In cases where the silylated heterocycles needed more drastic reaction conditions the use of the stannylated heterocycles was indicated. In the reaction of benzothiazol-2-yltrimethyl-stannane (6) with ...

Related Articles:

Regioselectivity in the addition of vinylmagnesium bromide to heteroarylic ketones: C-versus O-alkylation

[Boga, Carla; Forlani, Luciano; Todesco, Paolo E. Gazzetta Chimica Italiana, 1997 , vol. 127, # 4 p. 197 - 200]

C??Acylierung von 5 gliedrigen N??Heterocyclen, II. Acylierung von 1??Acylimidazolen, Thiazolen und Oxazolen sowie Darstellung N??unsubstituierter C??Acylazole

[Regel,E. Justus Liebigs Annalen der Chemie, 1977 , p. 159 - 168]

Synthesis of 1-formyldipyrromethanes

[Nagasaki, Izuru; Suzuki, Yumiko; Iwamoto, Ken-Ichi; Higashino, Takeo; Miyashita, Akira Heterocycles, 1997 , vol. 46, # 1 p. 443 - 450]

More Articles...