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Synthesis of Some amino-4,5-dihydropyrazolo[3,4-a]acridines as potential cholinesterase inhibitors

โœ 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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๐Ÿ“œ SIMILAR VOLUMES


Synthesis of 5-amino-4, 5-dihydropyrazol
โœ A. Maquestiau; J.-J. Vanden Eynde ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 572 KB

## 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.

Synthesis of 2-amino-4-oxo-5-substituted
โœ Aleem Gangjee; Hiteshkumar D. Jain; Jaclyn Phan; Roy L. Kisliuk ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 59 KB

A series of ten novel 2-amino-4-oxo-5-[(substitutedbenzyl)thio]pyrrolo [2,3-d]pyrimidines 2-11 were synthesized as potential inhibitors of thymidylate synthase and as antitumor agents. The analogues contain various electron withdrawing and electron donating substituents on the benzylsulfanyl ring of