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The Alder-ene reaction is a chemical reaction between an alkene with an allylic hydrogen, and it provides an efficient method to construct the C-C bond. Traditionally, this reaction requires catalysts, high temperatures, or photocatalysis. In this study, we reported a high-pressure-induced solid-state Alder-ene reaction of 1-hexene at room temperature without a catalyst. 1-Hexene crystallizes at 4.3 GPa and polymerizes at 18 GPa, forming olefins. By exploring gas chromatography-mass spectrometry, we discovered that 1-hexene generates dimeric products through the Alder-ene reaction under high pressures. The neutron diffraction shows that the reaction process did not obey the topochemical rule. A six-membered ring transition state including one C-H σ bond and two alkene π bonds was evidenced by the theoretical calculation, whose energy obviously decreased when compressed to 20 GPa. Our work offers a novel and promising method to realize the Alder-ene reaction at room temperature without a catalyst, expanding the application of this important reaction.
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http://dx.doi.org/10.1021/acs.jpclett.4c03696 | DOI Listing |
Beilstein J Org Chem
August 2025
Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, 28040-Madrid, Spain.
The influence of transition-state aromaticity on the barrier heights of concerted pericyclic reactions is summarized herein. To this end, selected representative examples ranging from fundamental processes such as Diels-Alder or Alder-ene reactions to double-group transfer reactions or 1,3-dipolar cycloadditions involving metal complexes are presented. It is found that while more synchronous processes tend to exhibit greater aromatic character in their transition states, this increased aromaticity does not necessarily correlate with lower activation barriers.
View Article and Find Full Text PDFChem Commun (Camb)
July 2025
School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, China.
A highly diastereoselective Pd-catalyzed sequential reaction of -iodophenyl-ynones, propargylic ethers and maleimides is developed for efficient synthesis of tetracyclic succinimide derivatives containing three contiguous stereocenters and one exocyclic double bond. The reaction proceeds through Pd-catalyzed cross-coupling and propargyl Alder-ene reactions to generate a reactive indenone-allene intermediate, which undergoes an intermolecular Diels-Alder cycloaddition with maleimide to deliver a densely functionalized product. In addition, a formal four-component reaction was observed for generating polycyclic products bearing two succinimide motifs.
View Article and Find Full Text PDFOrg Lett
June 2025
School of Chemistry and Chemical Engineering, Nanchang University, Nanchang 330031, P. R. China.
A Pd-catalyzed Sonogashira coupling of iodoalkynones with propargylic ethers bearing indole-tethered unactivated alkenes, followed by an Alder-ene reaction and a Diels-Alder cycloaddition, provides access to various hexacyclic heterocycles containing a dihydropyrido[1,2-]indole scaffold. When similar -propargylic allylic ethers were applied to the reaction, polycyclic compounds containing pyrido[1,2-]indole scaffolds could be obtained after treatment of the fused cyclic products with trifluoroacetic acid. The method features a broad substrate scope, high stereoselectivity, and mild reaction conditions.
View Article and Find Full Text PDFOrg Biomol Chem
June 2025
Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling, Shaanxi 712100, China.
A synthesis of the 6-5-5 tricyclic skeleton of the diterpenoid aberrarone is reported. The synthesis strategically features an intermolecular Diels-Alder reaction to construct the -hydrindane moiety and a cross-coupling-isomerization-intramolecular Alder-ene cyclization cascade to efficiently assemble the 6-5-5 tricyclic skeleton of aberrarone.
View Article and Find Full Text PDFJ Org Chem
May 2025
State Key Laboratory of Antiviral Drugs, NMPA Key Laboratory for Research and Evaluation of Innovative Drug, School of Chemistry and Chemical Engineering, Pingyuan Laboratory, Henan Normal University, Xinxiang 453007, China.
The Alder-ene reaction of the C-C bond in bicyclo[1.1.0]butanes would provide a unique and efficient synthesis route for cyclobutene frameworks.
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