Asymmetrie total synthesis of a natural product using catalytic enantioselective stereoablative reactions

Research output: Contribution to journalReview article

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 languageEnglish
Pages (from-to)166-168
Number of pages3
JournalYuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Volume67
Issue number2
Publication statusPublished - 2009 Feb
Externally publishedYes

Fingerprint

Diterpenes
Biological Products
Molecules
cyanthiwigin F

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

@article{346126a5d42c45e980cf2e997bf1dfdd,
title = "Asymmetrie total synthesis of a natural product using catalytic enantioselective stereoablative reactions",
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.",
author = "Junichiro Yamaguchi",
year = "2009",
month = "2",
language = "English",
volume = "67",
pages = "166--168",
journal = "Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry",
issn = "0037-9980",
publisher = "Society of Synthetic Organic Chemistry",
number = "2",

}

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.

UR - http://www.scopus.com/inward/record.url?scp=65449139187&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=65449139187&partnerID=8YFLogxK

M3 - Review article

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 -