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http://localhost:8080/xmlui/handle/123456789/3044Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Santhosh, P. | - |
| dc.contributor.author | Chunduru, V.S.R | - |
| dc.contributor.author | Rajeswar Rao, V. | - |
| dc.date.accessioned | 2025-01-31T11:03:23Z | - |
| dc.date.available | 2025-01-31T11:03:23Z | - |
| dc.date.issued | 2011 | - |
| dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/3044 | - |
| dc.description | NITW | en_US |
| dc.description.abstract | A regioselective enzyme-catalyzed system is selected for the synthesis of 1,3,5-trisubstituted pyrazole derivatives by adding phenyl hydrazines, nitroolefins, and benzaldehydes. The reaction is performed in a one-pot vessel with a yield ranging from 49 to 90%. TLL@MMI, immobilized Thermomyces lanuginosus lipase (TLL) on a multivariate of MOF-5/IRMOF-3 (MMI), showed good performance for the catalysis of this reaction. The prepared biocatalyst was characterized by FTIR, XRD, SEM, and EDX. The thermal and solvent stability of TLL@MMI was investigated in MeOH and EtOH after 24 h incubation. In the presence of 100% concentrations of EtOH, TLL@MMI has 80% activity | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Khimiya Geterotsiklicheskikh Soedinenii | en_US |
| dc.subject | Catalysts | en_US |
| dc.subject | Ethanol | en_US |
| dc.title | One-pot synthesis of trisubstituted pyrazoles via multicomponent approach | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Chemistry | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| rangraz-et-al-2024-one-pot-synthesis-of-1-3-5-trisubstitued-pyrazoles-via-immobilized-thermomyces-lanuginosus-lipase.pdf | 5.11 MB | Adobe PDF | View/Open |
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