Cyclopropanation of. alpha.,. beta.-unsaturated carbonyl compounds and nitriles with diazo compounds. The nature of the involvement of transition-metal promoters
MP Doyle, RL Dorow, WH Tamblyn
Index: Doyle, Michael P.; Dorow, Roberta L.; Tamblyn, William H. Journal of Organic Chemistry, 1982 , vol. 47, # 21 p. 4059 - 4068
Full Text: HTML
Citation Number: 68
Abstract
In the presence of molybdenum hexacarbonyl or molybdenum (I1) acetate, ethyl diazoacetate and a-diazoacetophenone react with a,@-unsaturated carbonyl compounds and nitriles to form derivative cyclopropane and vinyl CH insertion products. In the abrrence of these promoters or in the presence of catalytic amounts of pyridine, 2-pyrazolines are the major or sole reaction products. Kinetic investigations for reactions between ethyl ...
Related Articles:
Effective methods for the syntheses of 2??pyrazolines and pyrazoles from diazocarbonyl compounds
[Doyle, Michael P.; Colsman, Mark R.; Dorow, Roberta L. Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 943 - 946]