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dc.contributor.authorLohray, B B-
dc.contributor.authorBhushan, Vidya-
dc.contributor.authorReddy, A Sekar-
dc.contributor.authorRao, V Venugopal-
dc.date.accessioned2013-10-23T04:57:41Z-
dc.date.available2013-10-23T04:57:41Z-
dc.date.issued2000-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22511-
dc.description297-299en_US
dc.description.abstractSeveral tricyclic [6:6:5] and [6 :7:5] systems 2a-f have been synthesized from the corresponding amido esters 1a-f. The possible mechanistic pathways have been suggested for the LAH reduction of 1a-f and are based on the products distribution.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.39B(04) [April 2000]en_US
dc.titleNovel method for the preparation of tricyclic [6:6:5] systems by reductive cyclisation with LAHen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(04) [April 2000]

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