Abstract
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.
Original language | English |
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Pages (from-to) | 166-168 |
Number of pages | 3 |
Journal | Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry |
Volume | 67 |
Issue number | 2 |
Publication status | Published - 2009 Feb |
Externally published | Yes |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
Asymmetrie total synthesis of a natural product using catalytic enantioselective stereoablative reactions. / Yamaguchi, Junichiro.
In: Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, Vol. 67, No. 2, 02.2009, p. 166-168.Research output: Contribution to journal › Review article
}
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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UR - http://www.scopus.com/inward/citedby.url?scp=65449139187&partnerID=8YFLogxK
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 -