New tetralone acid intermediates for the synthesis of β-apopicropodophyllin analogues.

Sadashivamurthy, B. and Basavaraju, Y. B. and Sathisha, A. D. and Hemakumar, K. H. (2007) New tetralone acid intermediates for the synthesis of β-apopicropodophyllin analogues. Bulgarian Chemical Communications, 39 (4, Cop). pp. 264-268. ISSN 0324-1130

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Abstract

New tetralone acid intermediates 3-carboxy-4-(p-tolyl)-6,7-dimethoxy-1-tetralone, 3-carboxy-4-(p-tolyl)-6-methyl-7-methoxy-1-tetralone and 3-carboxy-4-(p-tolyl)-6-chloro-7-methoxy-1-tetralone were synthesized in high yields by Gensler's route with some change in reagents. They are very essential for the synthesis and study of antimitotic activity of β-apopicropodophyllin analogs. All the products were characterized by spectral and elemental anal. data. [on SciFinder(R)]

Item Type: Article
Additional Information: Unmapped bibliographic data: PY - 2007/// [EPrints field already has value set] JA - Bulg. Chem. Commun. [Field not mapped to EPrints]
Uncontrolled Keywords: stereoselective synthesis tetralone acid intermediate redn Friedel Crafts acylation
Subjects: Physical Sciences > Chemistry
Divisions: PG Campuses > Manasagangotri, Mysore > Chemistry
Depositing User: Dhruvakumar
Date Deposited: 11 Jun 2013 10:04
Last Modified: 11 Jun 2013 10:04
URI: http://eprints.uni-mysore.ac.in/id/eprint/12377

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