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A simple approach for the synthesis of azocine alkaloids: The total synthesis of megallanesine

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dc.contributor.author Volvoikar, P.S.
dc.contributor.author Tilve, S.G.
dc.date.accessioned 2018-06-12T04:38:46Z
dc.date.available 2018-06-12T04:38:46Z
dc.date.issued 2018
dc.identifier.citation Tetrahedron Letters. 59(26); 2018; 2567-2569. en_US
dc.identifier.uri https://doi.org/10.1016/j.tetlet.2018.05.055
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/5247
dc.description.abstract A new three step synthetic route to construct azocine ring system using anion chemistry and intramolecular Friedel-Craft reaction of an ester is presented. This method allows synthesis of azocine ring analogues in excellent overall yields. The designed strategy was applied for the synthesis of naturally occurring magallanesine. en_US
dc.publisher Elsevier en_US
dc.subject Chemistry en_US
dc.title A simple approach for the synthesis of azocine alkaloids: The total synthesis of megallanesine en_US
dc.type Journal article en_US
dc.identifier.impf y


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