Asymmetric total syntheses of panaxytriol and panaxydol, potent antitumor agents from Panax ginseng

A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d-arabinose using base induced double elimination of 4,5- O-isopropylidene propargyl chloride as a key step is described. Graphic

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Published in:Tetrahedron Vol. 58; no. 24; pp. 4955 - 4961
Main Authors: Yadav, J.S, Maiti, Arup
Format: Journal Article
Language:English
Published: Elsevier Ltd 10-06-2002
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Abstract A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d-arabinose using base induced double elimination of 4,5- O-isopropylidene propargyl chloride as a key step is described. Graphic
AbstractList A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d-arabinose using base induced double elimination of 4,5- O-isopropylidene propargyl chloride as a key step is described. Graphic
Author Yadav, J.S
Maiti, Arup
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Keywords Panax ginseng
panaxytriol
asymmetric total synthesis
Language English
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  start-page: 162
  year: 1983
  ident: 10.1016/S0040-4020(02)00423-4_BIB3_2
  publication-title: Yakugaku Zasshi
  contributor:
    fullname: Kitagawa
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Snippet A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d-arabinose using base induced double elimination of 4,5- O-isopropylidene propargyl chloride...
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SubjectTerms asymmetric total synthesis
Panax ginseng
panaxytriol
Title Asymmetric total syntheses of panaxytriol and panaxydol, potent antitumor agents from Panax ginseng
URI https://dx.doi.org/10.1016/S0040-4020(02)00423-4
Volume 58
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