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dc.contributor.authorKadam, A J-
dc.contributor.authorBaraskar, U K-
dc.contributor.authorMane, R B-
dc.date.accessioned2013-10-23T09:46:08Z-
dc.date.available2013-10-23T09:46:08Z-
dc.date.issued2000-11-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22566-
dc.description822-825en_US
dc.description.abstract7-Methoxy-6-methyl-1-tetralone 6 on Wolff-Kishner reduction followed by chromic acid oxidation furnishes tetralone 8 which on Grignard reaction with isopropylmagnesium iodide yields 6-methoxy-7-methyl-1-isopropyltetralol 9. The tetralol 9 on hydrogenation over Pd-C gives 7-methoxynorcalamenene 1. The tetralone 6 on reaction with methylmagnesium iodide followed by hydrogenation over Pd-C affords tetralin 12. The chromic acid oxidation of 12 furnishes 4,7-dimethyl-6-methoxytetralone 2. The telralone 2 on Grignard reaction with isopropylmagnesium iodide yields tetralol 13 which on hydrogenation over Pd-C affords(±) -7-methoxycalamenene 3.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(11) [November 2000]en_US
dc.titleSynthesis of 7 -methoxynorcalamenene, 4, 7 -dimethyl-6-methoxytetralone and 7-methoxycalameneneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(11) [November 2000]

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