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pubmed-article:7670191pubmed:abstractTextThe absolute stereochemistry of yeast reduction products 2s and 2a from 2-(3',4'-dimethoxy-cinnamyl)-2-methylcyclopentane-1,3-dione (1) was investigated. The results from several spectral studies and chemical correlations enabled their absolute configurations to be concluded as (2S,3S) and (2R,3S), respectively.lld:pubmed
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pubmed-article:7670191pubmed:articleTitleAbsolute stereochemistry of yeast reduction products from 2-(3',4'-dimethoxy-cinnamyl)-2-methylcyclopentane-1,3-dione.lld:pubmed
pubmed-article:7670191pubmed:affiliationPharmaceutical Research Laboratories, Kirin Brewery Co., Ltd., Gunma, Japan.lld:pubmed
pubmed-article:7670191pubmed:publicationTypeJournal Articlelld:pubmed