Preparation and reactions of mono??reissert compounds and analogs at the 3, 4??position of quinazoline
J Kant, FD Popp, BC Uff
Index: Kant, Joydeep; Popp, Frank D.; Uff, Barrie C. Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 1313 - 1316
Full Text: HTML
Citation Number: 4
Abstract
Abstract Quinazoline, acid chlorides, and trimethylsilyl cyanide have been converted to mono-Reissert compounds at the 3, 4-position of the quinazoline system. Various reactions of these quinazoline Reissert compounds are reported.
Related Articles:
[Alzogaray; Fontan; Camps; Masuh; Santo Orihuela; Fernandez; Cork; Zerba Molecules, 2005 , vol. 10, # 9 p. 1190 - 1196]
[Hahn, Jung-Tai; Popp, Frank D. Journal of Heterocyclic Chemistry, 1989 , vol. 26, p. 1357 - 1372]
[Singh, Harjit; Aggarwal, Sunil K.; Malhotra, Nageshwar Tetrahedron, 1986 , vol. 42, # 4 p. 1139 - 1144]
[Higashino, Takeo; Kokubo, Hiroyasu; Hayashi, Eisaku Chemical & Pharmaceutical Bulletin, 1985 , vol. 33, # 3 p. 950 - 961]
[Hahn, Jung-Tai; Popp, Frank D. Journal of Heterocyclic Chemistry, 1989 , vol. 26, p. 1357 - 1372]