Biomimetic synthesis of (-)-pycnanthuquinone C through the diels-alder reaction of a vinyl quinone

Florian Löbermann; Peter Mayer; Dirk Trauner

doi:10.1002/anie.201001862

Biomimetic synthesis of (-)-pycnanthuquinone C through the diels-alder reaction of a vinyl quinone

Florian Löbermann, Peter Mayer, Dirk Trauner

Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Three strikes and you're out! A concise, asymmetric synthesis of pycnanthuquinone C underscores the biosynthetic relevance of Diels-Alder reactions of vinyl quinones. The relative and absolute configuration of the natural product has been elucidated.

Original language	English (US)
Pages (from-to)	6199-6202
Number of pages	4
Journal	Angewandte Chemie - International Edition
Volume	49
Issue number	35
DOIs	https://doi.org/10.1002/anie.201001862
State	Published - Aug 16 2010

Keywords

Biomimetic synthesis
Diels-Alder reactions
Pycnanthuquinones
Total synthesis
Vinyl quinones

ASJC Scopus subject areas

Catalysis
General Chemistry

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10.1002/anie.201001862

Cite this

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abstract = "Three strikes and you're out! A concise, asymmetric synthesis of pycnanthuquinone C underscores the biosynthetic relevance of Diels-Alder reactions of vinyl quinones. The relative and absolute configuration of the natural product has been elucidated.",

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AU - Mayer, Peter

AU - Trauner, Dirk

PY - 2010/8/16

Y1 - 2010/8/16

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KW - Pycnanthuquinones

KW - Total synthesis

KW - Vinyl quinones

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Biomimetic synthesis of (-)-pycnanthuquinone C through the diels-alder reaction of a vinyl quinone

Abstract

Keywords

ASJC Scopus subject areas

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