1992
DOI: 10.1248/cpb.40.907
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Preparation of 5-Alkyl-3-carboxymethylrhodanines and Their Aldose Reductase Inhibitory Activity.

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Cited by 7 publications
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“…7 In contrast to literature reports, efforts to reduce 11 with sodium borohydride in DMF at 0°C failed to produce any of the desired product. 8 ammonium acetate provided the corresponding alkene in a 1:10 ratio of geometrical isomers by 1 H NMR. Based on literature precedence the isomeric ratio was presumed to be mainly the Z stereoisomer.…”
mentioning
confidence: 99%
“…7 In contrast to literature reports, efforts to reduce 11 with sodium borohydride in DMF at 0°C failed to produce any of the desired product. 8 ammonium acetate provided the corresponding alkene in a 1:10 ratio of geometrical isomers by 1 H NMR. Based on literature precedence the isomeric ratio was presumed to be mainly the Z stereoisomer.…”
mentioning
confidence: 99%