The Willgerodt Reaction. I. The Use of Aliphatic Carbonyl Compounds1
L Cavalieri, DB Pattison, M Carmack
Index: Cavalieri; Pattison; Carmack Journal of the American Chemical Society, 1945 , vol. 67, p. 1785
Full Text: HTML
Citation Number: 20
Abstract
Numerous examples of the use of the Willgerodt reaction with aryl alkyl ketones have appeared in the literature. 8,'Practically all of the successful reactions can be represented by the generalized equation in which the aryl group may be any of a wide variety of aromatic nuclei not affected by the reagent, and n may vary from 0 to at least 4. The reaction is caused by the action of aqueous ammonium polysulfide on the ketone in a closed system at ...
Related Articles:
[Tinnis, Fredrik; Lundberg, Helena; Adolfsson, Hans Advanced Synthesis and Catalysis, 2012 , vol. 354, # 13 p. 2531 - 2536]
The Addition of Silicon Hydrides to Olefinic Double Bonds. Part VI. Addition to Branched Olefins
[Saam,J.; Speier,J. Journal of the American Chemical Society, 1961 , vol. 83, p. 1351 - 1355]
Selektive Synthesen der endo??und exo??Norcaran??carbonsäuren??(7)
[Musso,H. Chemische Berichte, 1968 , vol. 101, p. 3710 - 3720]
The Addition of Silicon Hydrides to Olefinic Double Bonds. Part VI. Addition to Branched Olefins
[Saam,J.; Speier,J. Journal of the American Chemical Society, 1961 , vol. 83, p. 1351 - 1355]