Addition of titanium ester enolates to aldimines containing a chiral α-methylbenzylamine moiety: synthesis of chiral syn-β-amino esters

dc.contributor.author Periasamy, Mariappan
dc.contributor.author Suresh, Surisetti
dc.contributor.author Subramaniapillai, Selva Ganesan
dc.date.accessioned 2022-03-27T09:08:23Z
dc.date.available 2022-03-27T09:08:23Z
dc.date.issued 2006-05-15
dc.description.abstract Addition of titanium ester enolates to N-arylidene derivatives containing a (R)-α-methylbenzylamine moiety afforded (2S,3S,αR)-β-amino esters in 73-93% yields with 86:14 to 96:4 diastereomeric ratios. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Asymmetry. v.17(9)
dc.identifier.issn 09574166
dc.identifier.uri 10.1016/j.tetasy.2006.04.032
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0957416606002916
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12478
dc.title Addition of titanium ester enolates to aldimines containing a chiral α-methylbenzylamine moiety: synthesis of chiral syn-β-amino esters
dc.type Journal. Article
dspace.entity.type
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