Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita–Baylis–Hillman carbonates to access polysubstituted furans and cyclopentenes

Chemical Communications, Год журнала: 2024, Номер 60(27), С. 3717 - 3720

Опубликована: Янв. 1, 2024

The substrate-enabled switching of the regioselectivity allows for efficient regiocontrol via [4+1] and [3+2] annulations ninhydrin-derived MBH carbonates with α,β-unsaturated ketones to access highly substituted furans cyclopentene.

Язык: Английский

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Cooperative Gold(I)/DMAP Catalysis Enabled (2 + 3) Cycloadditions of Yne–Enones with Oxindole-Derived MBH Carbonates

Organic Letters, Год журнала: 2024, Номер 26(18), С. 3790 - 3795

Опубликована: Апрель 26, 2024

A cooperative gold(I)/DMAP system catalyzes the (2 + 3) cycloadditions of yne-enones with oxindole-derived Morita-Baylis-Hillman (MBH) carbonates, yielding diverse bispiro-cyclopentene oxindole products. The mild, scalable protocol demonstrates broad substrate scope and excellent chemo- diastereoselectivity. Mechanistic study reveals pivotal roles both catalysts in unique cycloaddition. This strategy showcases superiority achieving transformation chemoselectivity diastereoselectivity, unattainable through traditional monocatalytic methodologies.

Язык: Английский

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Asymmetric palladium-catalyzed decarboxylative [3 + 2] cycloaddition: straightforward construction of chiral spiro-heterocyclic scaffolds

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(5), С. 1479 - 1483

Опубликована: Янв. 1, 2024

We developed an asymmetric Pd-catalyzed [3 + 2] cycloaddition of α,β-unsaturated pyrazolones with vinylethylene carbonates. An array spiro-tetrahydrofuran-pyrazolones were obtained in high yields excellent enantioselectivities.

Язык: Английский

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Construction of 3,4-Dihydroquinolone Derivatives through Pd-Catalyzed [4+2] Cycloaddition of Vinyl Benzoxazinanones with α-Alkylidene Succinimides

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(5), С. 3279 - 3291

Опубликована: Фев. 20, 2024

The construction of 3,4-dihydroquinolone derivatives has attracted a considerable amount attention due to their extensive applications in medicinal chemistry. In this study, we present the Pd-catalyzed [4+2] cycloaddition vinyl benzoxazinanones with α-alkylidene succinimides for efficient synthesis 3,4-dihydroquinolones. This approach presents numerous advantages, including ready availability starting materials, mild reaction conditions without use additional bases, and wide range substrates. particular, all desired products can be easily afforded high yields (≤99%) excellent diastereoselectivities (>20:1). practicality reliability strategy were demonstrated by successful scale-up subsequent straightforward synthetic transformations.

Язык: Английский

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Lewis Base Controlled (4 + 3) and (4 + 2) Annulations of MBH Carbonates with Benzofuran‐derived Azadienes: Access to Highly Substituted Benzofuro[3,2‐b]azepines and Spirotetrahydroquinolines

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(21), С. 4521 - 4527

Опубликована: Авг. 7, 2024

Abstract Catalyst‐controlled switchable (4+3) and (4+2) annulation reactions of Morita–Baylis–Hillman carbonates with benzofuran‐derived azadienes have been established. Employing PCy 3 as the catalyst, reaction could provide a variety synthetically useful benzofuro[3,2‐ b ]azepines in good yields (80–92%) excellent chemo‐ regioselectivities via cycloaddition reactions. Whereas changing catalyst from to DMAP, were switched construct highly substituted spirotetrahydroquinoline scaffolds three sequential stereocenters containing all‐carbon spiro‐quaternary efficiency diastereoselectivities (92–96% all cases>25:1 dr ) annulations. In addition, synthetic utility this method was further showcased by gram‐scale transformations product.

Язык: Английский

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Catalyst-controlled regiodivergence and stereodivergence in formal cross-[4+2] cycloadditions: The unique effect of bismuth(III)

Science Advances, Год журнала: 2025, Номер 11(13)

Опубликована: Март 26, 2025

The [4+2] cycloaddition is crucial for constructing six-membered rings in pharmaceuticals and natural products. Cross-[4+2] cycloadditions offer greater product diversity than traditional diene-dienophile reactions due to multiple possible pathways. However, precise control over regio- stereoselectivity various isomers remains a great challenge. This study reports catalyst-controlled regiodivergent formal cross-cycloadditions of acyclic dienes enones, significantly enhancing access diverse pyrazole-fused spirooxindoles. Chiral phosphoric acid (CPA) catalysis enables endoselective cycloadditions, while Bi(III) with CPA ligand yields [2+4] products high stereoselectivity. A Claisen rearrangement the adduct produces exo-selective product, further increasing stereochemical enabling synthesis six stereo-isomers from single substrate set. DFT calculations reveal that reverses regioselectivity by repositioning reactants pocket stabilizing enone oxygen’s negative charge. In addition, 3as demonstrates therapeutic potential against triple-negative breast cancer, an IC 50 8.5 μM MDA-MB-453 cells.

Язык: Английский

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Visible-light-induced C–S bond formation of pyrazolin-5-ones with thioureas to pyrazol-4-yl carbamimidothioates

Molecular Catalysis, Год журнала: 2025, Номер 580, С. 115086 - 115086

Опубликована: Апрель 8, 2025

Язык: Английский

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Catalyst-Controlled Divergent Synthesis of Bicyclo[2.1.1]hexanes and Cyclobutenes: The Unique Effect of Au(I)

JACS Au, Год журнала: 2025, Номер unknown

Опубликована: Май 22, 2025

Язык: Английский

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DMAP‐Catalyzed [4 + 3] Spiroannulation of Ninhydrin‐Derived MBH Carbonates with Acyclic Azadienes: Efficient Access to Multisubstituted Spiro[indanone‐azepine] Scaffolds

Asian Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Май 22, 2025

Abstract Indanedione‐containing spirocyclic derivatives are of significant interest in medicinal chemistry. However, spirofusion indanediones with seven‐membered rings remains relatively unexplored. In this study, we report an efficient DMAP‐catalyzed [4 + 3] annulation ninhydrin‐derived MBH carbonates acyclic azadienes, providing a series polysubstituted, pharmacologically interesting spiro[indanone‐azepine] good to excellent yields (up 98%) under mild conditons. The method is practical, tolerant various functional groups, and allows for the rapid synthesis diverse range products from simple, readily available starting materials. successful scale‐up reaction derivatization product further demonstrate practicality reliability method.

Язык: Английский

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Chemoselective synthesis of bridged benzo[no]tetraphen-8-one via copper-catalyzed radical dimerization of 1-alkynylnaphthols

Tetrahedron Letters, Год журнала: 2024, Номер 136, С. 154929 - 154929

Опубликована: Янв. 26, 2024

Язык: Английский

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