| dc.contributor.author | Kumar, Indresh | |
| dc.date.accessioned | 2021-10-27T04:28:24Z | |
| dc.date.available | 2021-10-27T04:28:24Z | |
| dc.date.issued | 2010-11 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0957416610007366?via%3Dihub | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3184 | |
| dc.description.abstract | A l-proline catalyzed direct diastereoselective 6-enolexo aldolization reaction of differentiating dialdehydes derived from tartaric acid is presented. This organocatalytic approach provides high levels of syn-selectivity (dr >10:1) with the stereocontrolled C–C bond formation between C4 and C5 intramolecularly, which can serve to synthesize imino-sugar skeleton quickly. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Elsiever | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Proline catalyzed | en_US |
| dc.subject | Diastereoselective | en_US |
| dc.subject | Synthesis | en_US |
| dc.title | Proline catalyzed direct diastereoselective 6-enolexo aldolization: toward the synthesis of the imino sugar DNJ | en_US |
| dc.type | Article | en_US |
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