Acid-catalysed cyclisation of 2-methyl-2[3-(2,4-dimethoxyphenyl)-5-methoxypent-2-enyl]-cyclopentane-1,3-dione: Structure of a novel product
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
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2. Rearrangement of homobrendane derivatives. Total syntheses of racemic copacamphor, ylangocamphor, and their homologs;The Journal of Organic Chemistry;1988-07
3. Rearrangement of a homobrendane to a perhydro-1,4-methanoindene skeleton. X-Ray crystal structure of a novel product;Journal of the Chemical Society, Chemical Communications;1987
4. Structures of some unusual types of organic compounds;Proceedings / Indian Academy of Sciences;1984-05
5. Acid-catalysed cyclisations: structures of novel products isolated in the reaction of 2-[3-(2,6-dimethoxyphenyl)but-2-enyl]-2-methylcyclopentane-1,3-dione with MeOH–HCl;J. Chem. Soc., Perkin Trans. 1;1982
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