| dc.contributor.author | Kumar, Indresh | |
| dc.date.accessioned | 2021-10-27T04:28:07Z | |
| dc.date.available | 2021-10-27T04:28:07Z | |
| dc.date.issued | 2012 | |
| dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2012/cc/c2cc33103a | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3178 | |
| dc.description.abstract | A new method for asymmetric synthesis of 2,3-substituted pyrrolidines from N-PMP aldimines and succinaldehyde via formal [3+2] cycloaddition is reported. This reaction involves proline catalyzed direct Mannich reaction and acid catalyzed reductive cyclization with high yields (up to 78%) and excellent enantioselectivities (up to >99%). | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | RSC | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Organocatalytic | en_US |
| dc.subject | Mannich–cyclization | en_US |
| dc.subject | Pyrrolidines | en_US |
| dc.title | An organocatalytic direct Mannich–cyclization cascade as [3+2] annulation: asymmetric synthesis of 2,3-substituted pyrrolidines | en_US |
| dc.type | Article | en_US |
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