Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219273 | Tetrahedron | 2012 | 7 Pages |
Abstract
A mild and highly regioselective synthesis of 1-acyl-5-hydroxypyrazolines has been achieved through the condensation of 1,2-allenic ketones with hydrazides in the absence of any catalyst. Moreover, the obtained 1-acyl-5-hydroxypyrazolines can be easily transformed into 1-acyl pyrazoles under the promotion of BF3·Et2O. It was also found that 1-acyl pyrazoles can be produced directly from allenic ketones and hydrazides through a one-pot procedure.
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