## Reactions between aminopyrazole-4-carboxylic acids derivatives and orthoesters or amide acetals lead, in most cases, to the introduction of a heteroalkylidene moiety on the amino group of ethyl aminopyrazole-4-carboxylates and on the p-hydrazide nitrogen atom of aminopyrazole-4-carboxhydrazides.
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Synthesis of Some amino-4,5-dihydropyrazolo[3,4-a]acridines as potential cholinesterase inhibitors
โ Scribed by Gregory M. Shutske; John D. Tomer IV
- Book ID
- 112130538
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1993
- Tongue
- English
- Weight
- 364 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0022-152X
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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