ChemInform Abstract: Synthesis and Antiaggregating Activity of 3-Aminopiperidine-2,6-dione and 3-Aminopyrrolidine-2,5-dione Derivatives.
β Scribed by A. A. KRYS'KO; V. M. KABANOV; T. A. KABANOVA; M. V. BELIKOVA; A. V. MAZEPA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Synthesis and Antiaggregating Activity of 3-Aminopiperidine-2,6dione and 3-Aminopyrrolidine-2,5-dione Derivatives.
-Several substituted 3-aminopiperidine-2,6-diones as well as their pyrrolidine analogues [cf. (VI), (VIII)] are prepared via reaction of anhydrides derived from N-Boc-protected 2-aminoalkanedioic acids (III) with pyridylamines (IV). All the compounds obtained inhibit the aggregation of thrombocytes. It is shown that introduction of the N-pyridyl group into the piperidinediones or pyrrolidinediones generally increases the antiaggregating activity as compared to the parent compounds such as (II). -(KRYS'
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v