Catalytic Enantioselective Diels–Alder Reaction of Dienes with Acyclic and α,β- and β,β-Disubstituted Enones

Despite the wealth of methods to enantioselectively catalyze Diels-Alder reactions of α,β-unsaturated carbonyl dienophiles, until today, not a single example with an acyclic enone that is either β,β- or α,β-disubstituted has been reported. Herein, we disclose a general Brønsted acid-catalyzed enantioselective Diels-Alder reaction of various aliphatic acyclic disubstituted enones with hydrocarbon dienes featuring diverse steric and electronic properties. The established method has been employed to synthesize several enantiopure targets, including well-known fragrance components such as arborone and the damascones.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-20
DOI
https://doi.org/10.1021/jacs.5c13725
Citations
2
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
1.87
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article

Catalytic Enantioselective Diels–Alder Reaction of Dienes with Acyclic and α,β- and β,β-Disubstituted Enones

Philip Kraft, Jan Samsonowicz‐Górski, Nils Nöthling, Santanu Ghosh et al.
2 citations
Journal of the American Chemical Society
Asymmetric Synthesis and Catalysis
1.87
article

Catalytic Enantioselective Diels–Alder Reaction of Dienes with Acyclic and α,β- and β,β-Disubstituted Enones

Philip Kraft, Jan Samsonowicz‐Górski, Nils Nöthling, Santanu Ghosh, Nobuya Tsuji, Benjamin List, Georg Breitenbruch, Markus Leutzsch
article en
2 citations

Abstract

Despite the wealth of methods to enantioselectively catalyze Diels-Alder reactions of α,β-unsaturated carbonyl dienophiles, until today, not a single example with an acyclic enone that is either β,β- or α,β-disubstituted has been reported. Herein, we disclose a general Brønsted acid-catalyzed enantioselective Diels-Alder reaction of various aliphatic acyclic disubstituted enones with hydrocarbon dienes featuring diverse steric and electronic properties. The established method has been employed to synthesize several enantiopure targets, including well-known fragrance components such as arborone and the damascones.

Journal of the American Chemical SocietyVol. 147(43)
Hokkaido University (JP), Max-Planck-Institut für Kohlenforschung (DE), Symrise (Germany) (DE)
Openalex Percentile: Top 13%
Asymmetric Synthesis and Catalysis
1.87
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