51304-72-4Relevant articles and documents
Palladium-catalyzed cross-coupling of aryl chlorides and tosylates with hydrazine
Lundgren, Rylan J.,Stradiotto, Mark
supporting information; experimental part, p. 8686 - 8690 (2011/01/08)
Hydrazine is not a problem anymore: The title transformation is the first reaction to yield aryl hydrazines through the cross-coupling of aryl chlorides and tosylates with hydrazine. An appropriately designed palladium catalyst allows this reaction to proceed rapidly under mild conditions, and with excellent chemoselectivity (see scheme; Ad=adamantyl, Ts=4-toluenesulfonyl).
Carbazole methyl malonates
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, (2008/06/13)
A process for the preparation of α-methyl-carbazole-2-acetic acids, which comprises reacting an α-methyl-3-oxocyclohexane malonic acid di-lower alkyl ester with a substituted phenylhydrazine, and thereafter sequentially oxidizing and hydrolyzing the reaction product to obtain the desired acid, is described.