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http://nopr.niscpr.res.in/handle/123456789/35171Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ganga, Venkata Subba Rao | - |
| dc.contributor.author | Abdi, Sayed H R | - |
| dc.contributor.author | Kureshy, Rukhsana I | - |
| dc.contributor.author | Khan, Noor-ul H | - |
| dc.contributor.author | Bajaj, Hari C | - |
| dc.date.accessioned | 2016-08-16T10:23:07Z | - |
| dc.date.available | 2016-08-16T10:23:07Z | - |
| dc.date.issued | 2016-08 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/35171 | - |
| dc.description | 950-955 | en_US |
| dc.description.abstract | L-Proline in the presence of benzoic acid is found to be an effective catalytic system for the cross-aldol condensation of benzaldehyde with 1-heptanal under solvent free condition amongst the several amino acids screened for this reaction. Under the optimized reaction conditions, the desired product (e.g. jasminaldehyde) is formed up to 96% selectivity in one hour using the desired arylaldehyde: 1-alkanaldehyde ratio as low as 2:1 under controlled addition of 1-alkanaldehyde. | 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-A Vol.55A(08) [August 2016] | en_US |
| dc.subject | Catalysis | en_US |
| dc.subject | Organocatalysts | en_US |
| dc.subject | Bifunctional organocatalysts | en_US |
| dc.subject | Cross-aldol condensation | en_US |
| dc.subject | Jasminaldehyde | en_US |
| dc.subject | Heptanal | en_US |
| dc.title | Bifunctional organocatalysts for the synthesis of jasminaldehyde and their derivatives | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.55A(08) [August 2016] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 55A(8) 950-955.pdf | 118.41 kB | Adobe PDF | View/Open |
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