Relative Cycloaddition Rates of Alkyne-Equivalent Dienophiles

Alkyne-equivalent dienophiles are strategically important coupling partners in Diels-Alder reactions. They are particularly useful in cascade bond-forming processes that begin with cycloadditions. A systematic rate study for the cycloaddition of several alkyne and alkyne-equivalent dienophiles is presented, showing that the relative reaction rates of these dienophiles vary over multiple orders of magnitude.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-03
DOI
https://doi.org/10.1021/acs.joc.4c03028
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Relative Cycloaddition Rates of Alkyne-Equivalent Dienophiles

Christopher M. Beaudry, Tucker J. Hamilton
The Journal of Organic Chemistry
Organic Chemistry Cycloaddition Reactions
article

Relative Cycloaddition Rates of Alkyne-Equivalent Dienophiles

Christopher M. Beaudry, Tucker J. Hamilton
article en

Abstract

Alkyne-equivalent dienophiles are strategically important coupling partners in Diels-Alder reactions. They are particularly useful in cascade bond-forming processes that begin with cycloadditions. A systematic rate study for the cycloaddition of several alkyne and alkyne-equivalent dienophiles is presented, showing that the relative reaction rates of these dienophiles vary over multiple orders of magnitude.

The Journal of Organic ChemistryVol. 90(14)
Oregon State University (US), Temple University (US)
Oregon State University, Division of Chemistry
Clean water and sanitation
Openalex Percentile: Top 95%
Organic Chemistry Cycloaddition Reactions
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