Cyclization of 3-diazoalkenes to pyrazoles
JL Brewbaker, H Hart
Index: Brewbaker,J.L.; Hart,H. Journal of the American Chemical Society, 1969 , vol. 91, # 3 p. 711 - 715
Full Text: HTML
Citation Number: 59
Abstract
Abstract: Eight 3-diazoalkenes have been prepared from the related ethyl alkenylnitrosocarbamates and methanolic sodium methoxide. All of these unsaturated diazo compounds spontaneously cyclized at room temperature to form pyrazoles in essentially quantitative yields. The cyclizations were cleanly unimolecular. The first-order rate constants for the reactions of four substituted trans-3-diazo-1-phenylpropenes fit the Hammett ...
Related Articles:
Two-stage sonogashira coupling method in the synthesis of auxin active acetylenes
[Wayne Craig; Eberle, Martin; Irminger, Bruno; Schueckenboehmer, Anegret; Laime, Yvette; Mueller, Patrick Heterocycles, 2007 , vol. 71, # 9 p. 1967 - 1974]
Oxidation of 1-aminopyrazoles and synthesis of 1, 2, 3-triazines
[Ohsawa, Akio; Arai, Heihachiro; Ohnishi, Hidefumi; Itoh, Takashi; Kaihoh, Terumitsu; et al. Journal of Organic Chemistry, 1985 , vol. 50, # 26 p. 5520 - 5523]
1, 3-Bisdiazopropane. Preparation and cyclization to pyrazole
[Hart,H.; Brewbaker,J.L. Journal of the American Chemical Society, 1969 , vol. 91, # 3 p. 706 - 711]
[Hsu, L.-Y.; Mariategui, J. F.; Niedenzu, K.; Shore, S. G. Inorganic Chemistry, 1987 , vol. 26, p. 143 - 147]
[Schneider; Goldbach Journal of the American Chemical Society, 1980 , vol. 102, # 19 p. 6114 - 6116]