ChemInform Abstract: A Regio- and Stereoselective 1,3-Dipolar Cycloaddition for the Synthesis of Novel Spiro-Pyrrolothiazolyloxindoles and Their Antitubercular Evaluation.
β Scribed by Pitchaimani Prasanna; Kamaraj Balamurugan; Subbu Perumal; Perumal Yogeewari; Dharmarajan Sriram
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 26 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Cycloaddition of azomethine ylides, generated in situ via decarboxylative condensation of isatins (II) and thiazolanecarboxylic acid (III) to indenones (I) provides the novel spiro compounds (IV).
π SIMILAR VOLUMES
Use of 1,3-Dipolar Cycloaddition for the Synthesis of Novel Fluoroquinolones. -A novel synthetic way for the modification of 6-fluoroquinoline-4-one-3-carboxylic acids is presented. The 7-azido-derivative (II) undergoes 1,3-dipolar cycloaddition to several alkenes like norbornene, cyclopentenonorbo
## 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