A new glucosinolate synthesis

  • Keller T
  • Yelland L
  • Benn M
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Abstract

The tert-butyldimethylsilyl nitronate derived from 1-nitropropane was condensed with 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylthiol to yield two geometrically isomeric thiohydroximates; the Z-isomeric form was then converted by conventional procedures into potassium ethylglucosinolate ("glucolepidiin").

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APA

Keller, T. H., Yelland, L. J., & Benn, M. H. (1984). A new glucosinolate synthesis. Canadian Journal of Chemistry, 62(3), 437–440. https://doi.org/10.1139/v84-075

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