Studies Toward Communesin F: A Diels-Alder Approach.

Jakob Danielsson; Peter Somfai

doi:10.1021/ol403516s

Studies Toward Communesin F: A Diels-Alder Approach.

Jakob Danielsson, Peter Somfai

Centre for Analysis and Synthesis

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

Abstract

A Diels-Alder reaction is used as a key step in a synthetic study toward communesin F, in order to simultaneously introduce both of the all-carbon quaternary stereocenters with complete control of relative stereochemistry. Further manipulations of the cycloadduct, toward the hexacyclic core-structure of communesin F, are also disclosed.

Original language	English
Pages (from-to)	784-787
Journal	Organic Letters
Volume	16
Issue number	3
DOIs	https://doi.org/10.1021/ol403516s
Publication status	Published - 2014

Subject classification (UKÄ)

Organic Chemistry

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10.1021/ol403516s

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title = "Studies Toward Communesin F: A Diels-Alder Approach.",

abstract = "A Diels-Alder reaction is used as a key step in a synthetic study toward communesin F, in order to simultaneously introduce both of the all-carbon quaternary stereocenters with complete control of relative stereochemistry. Further manipulations of the cycloadduct, toward the hexacyclic core-structure of communesin F, are also disclosed.",

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AB - A Diels-Alder reaction is used as a key step in a synthetic study toward communesin F, in order to simultaneously introduce both of the all-carbon quaternary stereocenters with complete control of relative stereochemistry. Further manipulations of the cycloadduct, toward the hexacyclic core-structure of communesin F, are also disclosed.

U2 - 10.1021/ol403516s

DO - 10.1021/ol403516s

M3 - Article

C2 - 24446678

SN - 1523-7052

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SP - 784

EP - 787

JO - Organic Letters

JF - Organic Letters

IS - 3

ER -

Studies Toward Communesin F: A Diels-Alder Approach.

Abstract

Subject classification (UKÄ)

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