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https://hdl.handle.net/10356/97497
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jin, Zhichao | en |
dc.contributor.author | Yang, Ruojie | en |
dc.contributor.author | Du, Yu | en |
dc.contributor.author | Tiwari, Bhoopendra | en |
dc.contributor.author | Ganguly, Rakesh | en |
dc.contributor.author | Chi, Robin Yonggui | en |
dc.date.accessioned | 2013-06-25T03:40:43Z | en |
dc.date.accessioned | 2019-12-06T19:43:19Z | - |
dc.date.available | 2013-06-25T03:40:43Z | en |
dc.date.available | 2019-12-06T19:43:19Z | - |
dc.date.copyright | 2012 | en |
dc.date.issued | 2012 | en |
dc.identifier.citation | Jin, Z., Yang, R., Du, Y., Tiwari, B., Ganguly, R., & Chi, Y. R. (2012). Enantioselective Intramolecular Formal [2 + 4] Annulation of Acrylates and α,β-Unsaturated Imines Catalyzed by Amino Acid Derived Phosphines. Organic Letters, 14(12), 3226-3229. | en |
dc.identifier.issn | 1523-7060 | en |
dc.identifier.uri | https://hdl.handle.net/10356/97497 | - |
dc.description.abstract | The first chiral phosphine-catalyzed activation of acrylates for intramolecular formal [2 + 4] reactions with unsaturated imines is described. The catalytic reactions afford N-heterocycles with exceptionally high diastereo- and enantioselectivities. The [2 + 4] products are amenable for further transformations to useful molecules such as chiral piperidines and multicyclic structures. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Organic letters | en |
dc.rights | © 2012 American Chemical Society. | en |
dc.title | Enantioselective intramolecular formal [2 + 4] annulation of acrylates and α,β-unsaturated imines catalyzed by amino acid derived phosphines | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1021/ol3013588 | en |
dc.identifier.rims | 173626 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | SPMS Journal Articles |
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