Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22566
Title: Synthesis of 7 -methoxynorcalamenene, 4, 7 -dimethyl-6-methoxytetralone and 7-methoxycalamenene
Authors: Kadam, A J
Baraskar, U K
Mane, R B
Issue Date: Nov-2000
Publisher: NISCAIR-CSIR, India
Abstract: 7-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.
Page(s): 822-825
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.39B(11) [November 2000]

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