Renewed Focus On A Neglected Reaction | October 15, 2012 Issue - Vol. 90 Issue 42 | Chemical & Engineering News
Volume 90 Issue 42 | p. 7 | News of The Week
Issue Date: October 15, 2012

Renewed Focus On A Neglected Reaction

Synthesis: New Diels-Alder route to complex benzenoids
Department: Science & Technology
News Channels: Organic SCENE
Keywords: hexadehydro-Diels-Alder (HDDA) reaction, Diels-Alder reaction, cycloaddition
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Nucleophilic reagents such as phenol substitute intermolecularly onto a reactive benzyne formed intramolecularly by alkyne-diyne cycloaddition, yielding complex benzenoid products. Dashed lines show benzyne-ring-forming interactions.
A reaction scheme showing how nucleophilic reagents substitute intermolecularly into a reactive benzyne formed intramolecularly by alkyne-diyne cycloaddition. Complex benzenoid products are the result of this reaction.
 
Nucleophilic reagents such as phenol substitute intermolecularly onto a reactive benzyne formed intramolecularly by alkyne-diyne cycloaddition, yielding complex benzenoid products. Dashed lines show benzyne-ring-forming interactions.

Researchers have found that a known cycloaddition reaction has not been living up to its potential. The finding could lead to more efficient syntheses of drugs, natural products, heteroaromatics, polyacenes, and other compounds.

The reaction is the Diels-Alder cycloaddition of an alkyne and diyne. Natural products specialist Thomas R. Hoye and coworkers at the University of Minnesota rediscovered serendipitously that mild heating of a starting material containing alkyne and diyne groups induces intramolecular Diels-Alder cycloaddition to benzyne, which is then trapped—for example, by an internal t-butyldimethylsiloxy group—to give polycyclic benzenoid products (Nature, DOI: 10.1038/nature11518).

The Hoye group also found that the benzyne intermediate can, in the absence of an internal trapping agent, react intermolecularly with reagents like alcohols, amides, halides, or acids to form complex benzenoids. They propose that the process that generates the reactive benzyne be renamed the hexadehydro-Diels-Alder (HDDA) reaction.

The first clear examples of the HDDA reaction were reported in 1997 by organic chemist Richard P. Johnson’s group at the University of New Hampshire and independently by organic chemist Ikuo Ueda and coworkers at Osaka University, in Japan. Recently, Brian T. Sterenberg’s group at the University of Regina, in Saskatchewan, reported a metal-templated version. But chemists have rarely used the reaction or exploited it for synthetic purposes.

What is most novel in the current study “is the beautiful intramolecular trapping by a proximate protecting group and a wide variety of intermolecular benzyne-trapping agents,” Johnson comments. “This is an important paper that may help a spectacular but long overlooked type of cycloaddition find its way into the synthetic lexicon.”

The work shows that the HDDA reaction, “previously primarily a curiosity, has significant synthetic applications,” says Sterenberg. “The relatively easy precursor synthesis along with the potential for further elaboration means that the reaction will find applications in the synthesis of complex polycyclic organic products. This paper will have a significant impact on the field of organic synthesis.”

 
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ISSN 0009-2347
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