TY - JOUR
T1 - Asymmetrie total synthesis of a natural product using catalytic enantioselective stereoablative reactions
AU - Yamaguchi, Junichiro
PY - 2009/2
Y1 - 2009/2
N2 - Catalytic enantioselective Stereoablative reactions represent a unique approach to the preparation of enantioenriched materials, wherein a catalytic method destroys, at least temporarily, stereogenic elements of a molecule. This review introduces a recent example of novel approaches in asymmetric catalytic methods for stereoablation, as well as the use of a new Stereoablative reaction in a concise synthesis of the marine diterpenoid (-)-cyanthiwigin F.
AB - Catalytic enantioselective Stereoablative reactions represent a unique approach to the preparation of enantioenriched materials, wherein a catalytic method destroys, at least temporarily, stereogenic elements of a molecule. This review introduces a recent example of novel approaches in asymmetric catalytic methods for stereoablation, as well as the use of a new Stereoablative reaction in a concise synthesis of the marine diterpenoid (-)-cyanthiwigin F.
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U2 - 10.5059/yukigoseikyokaishi.67.166
DO - 10.5059/yukigoseikyokaishi.67.166
M3 - Review article
AN - SCOPUS:65449139187
VL - 67
SP - 166
EP - 168
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
SN - 0037-9980
IS - 2
ER -