Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2535
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dc.contributor.authorNaveen-
dc.contributor.authorBabu, S.A.-
dc.date.accessioned2020-12-03T04:16:55Z-
dc.date.available2020-12-03T04:16:55Z-
dc.date.issued2016-
dc.identifier.citationTetrahedron Letters, 57(50), pp. 5690-5694en_US
dc.identifier.otherhttps://doi.org/10.1016/j.tetlet.2016.11.026-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403916314824-
dc.identifier.urihttp://hdl.handle.net/123456789/2535-
dc.description.abstractWe report the application of ring closing metathesis-based macrocyclization route for synthesizing 22–36 membered optically active aza-oxo crowns/polyether macrocycles. While the RCM-based synthesis of polyether macrocycles was well explored in the literature, the synthesis of optically active polyether macrocycles was not explored via the RCM reaction. Accordingly, the present method reveals an efficient assembling of a library of new classes of optically active aza-oxo polyether macrocycles from optically active RCM precursors, which were assembled from easily available linkers, chiral α-methylbenzylamine and amino alcohol building blocks under simple reaction conditions.en_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.subjectGrubbs’s catalysten_US
dc.subjectMacrocyclizationen_US
dc.subjectMacrocyclic olefinsen_US
dc.subjectAza-oxo polyether macrocyclesen_US
dc.subjectRing closing metathesisen_US
dc.titleAn entry into new classes of optically active aza-oxo polyether macrocycles via the ring closing metathesis-based macrocyclizationen_US
dc.typeArticleen_US
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