Pd-Catalyzed [2 + 2 + 2] Cyclization of Alkyne-cyclohexadienones and <i>O</i>-Akynyl Benzenesulfonamides for Construction of Fused Tricyclic Hydronaphthofurans

A palladium-catalyzed [2 + 2 + 2] cyclization of 1,6-enynes with unsymmetrical alkynes has been successfully accomplished, resulting in the formation of a series of fused tricyclic hydronaphthofurans with high stereo- and regioselectivity in a single step. This reaction demonstrates 100% atomic economy and exhibits a broad substrate scope.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-12-16
DOI
https://doi.org/10.1021/acs.joc.4c02447
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Pd-Catalyzed [2 + 2 + 2] Cyclization of Alkyne-cyclohexadienones and O-Akynyl Benzenesulfonamides for Construction of Fused Tricyclic Hydronaphthofurans

Junbiao Chang, Miaomiao Tian, Bingxian Liu, Xuxu Ma et al.
1 citations
The Journal of Organic Chemistry
Catalytic Alkyne Reactions
0.25
article

Pd-Catalyzed [2 + 2 + 2] Cyclization of Alkyne-cyclohexadienones and O-Akynyl Benzenesulfonamides for Construction of Fused Tricyclic Hydronaphthofurans

Junbiao Chang, Miaomiao Tian, Bingxian Liu, Xuxu Ma, Tianyun Zhang
article en
1 citations

Abstract

A palladium-catalyzed [2 + 2 + 2] cyclization of 1,6-enynes with unsymmetrical alkynes has been successfully accomplished, resulting in the formation of a series of fused tricyclic hydronaphthofurans with high stereo- and regioselectivity in a single step. This reaction demonstrates 100% atomic economy and exhibits a broad substrate scope.

The Journal of Organic ChemistryVol. 90(1)
Henan Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province, National Key Research and Development Program of China, Central Plains Scholars and Scientists Studio Fund
Openalex Percentile: Top 45%
Catalytic Alkyne Reactions
0.25
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