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https://hdl.handle.net/10356/104212
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Xu, Jianfeng | en |
dc.contributor.author | Jin, Zhichao | en |
dc.contributor.author | Chi, Robin Yonggui | en |
dc.date.accessioned | 2014-05-26T01:38:33Z | en |
dc.date.accessioned | 2019-12-06T21:28:30Z | - |
dc.date.available | 2014-05-26T01:38:33Z | en |
dc.date.available | 2019-12-06T21:28:30Z | - |
dc.date.copyright | 2013 | en |
dc.date.issued | 2013 | en |
dc.identifier.citation | Xu, J., Jin, Z., & Chi, Y. R. (2013). Organocatalytic Enantioselective γ-Aminoalkylation of Unsaturated Ester: Access to Pipecolic Acid Derivatives. Organic Letters, 15(19), 5028–5031. | en |
dc.identifier.issn | 1523-7060 | en |
dc.identifier.uri | https://hdl.handle.net/10356/104212 | - |
dc.description.abstract | The direct γ-carbon functionalization of α,β-unsaturated esters via N-Heterocyclic Carbene (NHC) catalysis is disclosed. This catalytically generated nucleophilic γ-carbon undergoes highly enantioselective additions to hydrazones. The resulting δ-lactam products can be readily transformed to optically enriched pipecolic acid derivatives. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Organic letters | en |
dc.rights | © 2013 American Chemical Society. | en |
dc.subject | DRNTU::Science::Chemistry::Organic chemistry | en |
dc.title | Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester : access to pipecolic acid derivatives | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1021/ol402358k | en |
dc.identifier.rims | 179769 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | SPMS Journal Articles |
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