Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/16217Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Gadaginamath, G S | - |
| dc.contributor.author | Shyadligeri, A S | - |
| dc.contributor.author | Kavali, R R | - |
| dc.date.accessioned | 2013-03-04T17:04:32Z | - |
| dc.date.available | 2013-03-04T17:04:32Z | - |
| dc.date.issued | 1999-02 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16217 | - |
| dc.description | 156-159 | en_US |
| dc.description.abstract | Exclusive formation of 3-carbethoxyindol-5-yloxyacetic acid hydrazides 3a,b from 3-carbethoxy-5- ethoxycarbonylmethoxyindoles 2a,b reveals the chemoselectivity of the C5-methyl ester function towards the nucleophilic attack of hydrazine hydrate. These mono hydrazides 3a,b on reacting with benzaldehydes furnish 1-alkyl-5- benzalhydrazinocarbonylmethoxy-3-ethoxycarbonyl-2-methylindoles 5a-h which on treatment with thioglycolic acid afford the desired 1-alkyl-3-ethoxycarbonyl-2-methyl-5-[(2-phenyl-4-thiazolidinon-3-yl)aminocarbonylmethoxy] indoles 6a-h. All the new compounds have been screened for their antibacterial and antifungal activities. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.38B(02) [February 1999] | en_US |
| dc.title | Chemoselectivity of indole-dicarboxylates towards hydrazine hydrate: Part III - Synthesis and antimicrobial activity of novel 4-thiazolidinonylindoles | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(02) [February 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(2) 156-159.pdf | 896.69 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.