Tetrahedron, Год журнала: 2024, Номер 169, С. 134378 - 134378
Опубликована: Ноя. 13, 2024
Язык: Английский
Tetrahedron, Год журнала: 2024, Номер 169, С. 134378 - 134378
Опубликована: Ноя. 13, 2024
Язык: Английский
ACS Catalysis, Год журнала: 2025, Номер unknown, С. 3184 - 3190
Опубликована: Фев. 6, 2025
A direct electroreductive functionalization of tropones employing aldehydes as alkylating agents is reported. This C(sp2)-H process leverages the mediation electroactive nickel complexes, enabling a wide range both native and substituted (44 examples) to be alkylated selectively at α-position in high yields (up 90%). Combined electrochemical, spectroelectrochemical, computational analyses disclosed whole mechanistic pathway revealed key role played by reduced Ni complexes activating tropone core toward condensation with aldehydes.
Язык: Английский
Процитировано
0Sustainable Chemistry and Pharmacy, Год журнала: 2025, Номер 44, С. 101957 - 101957
Опубликована: Март 3, 2025
Язык: Английский
Процитировано
0Organic Letters, Год журнала: 2025, Номер unknown
Опубликована: Март 17, 2025
Instead of the conventional [4+2] cycloaddition, a regioselective Schmittel-type [2+2] cycloaddition yne–allene esters, generated in situ from copper-catalyzed dediazotized coupling γ-alkynyl diazoacetates with terminal alkynes, is reported, enabling bicyclization process to produce diverse array C1-arylated cyclobuta[a]indenes moderate good yields. The protocol features wide functional group compatibility, mild reaction conditions, and experimental simplicity, holding significant potential for building new tricyclic cyclobutenes.
Язык: Английский
Процитировано
0Опубликована: Апрель 23, 2025
Язык: Английский
Процитировано
0Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
0Advanced Synthesis & Catalysis, Год журнала: 2024, Номер unknown
Опубликована: Окт. 9, 2024
Abstract [10+2]‐Hetero‐higher‐order cycloaddition between tropone hydrazides (acting as 10π‐components) and 3‐alkylidene oxindoles 2π‐components) has been established. Under Brønsted base catalysis the reaction proceeded in a fully peri‐ diastereoselective manner with stereochemical outcome governed mainly by electronic interactions. Following such strategy, series of structurally diverse tetrahydropyridazines were prepared 30–70% yields. Furthermore, potential obtained cycloadducts confirmed selected chemoselective transformations.
Язык: Английский
Процитировано
0ACS Catalysis, Год журнала: 2024, Номер 14(21), С. 16105 - 16114
Опубликована: Окт. 17, 2024
We introduce a phosphine-catalyzed cycloaddition involving unprecedented long-range intramolecular proton transfer, facilitating the synthesis of nine-membered heterocycles, which are privileged structures in natural products, as well potent pharmacophores. Experimental and computational studies revealed that enamide tether N-aromatic zwitterion directly enables regioselective transfer to proceed independently outer-sphere shuttling. This understanding selective has led improved efficiency regioselectivity desired 1,9-proton reaction under anhydrous conditions, thereby advancing development higher-order reactions. Further stereoselective contraction synthesized cyclic compounds using 3-aza-Cope rearrangement demonstrates synthetic versatility our approach. The findings this study not only advance general mechanism but also broaden its practical utility various chemical fields.
Язык: Английский
Процитировано
0Tetrahedron Chem, Год журнала: 2024, Номер unknown, С. 100103 - 100103
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
0Tetrahedron, Год журнала: 2024, Номер 169, С. 134378 - 134378
Опубликована: Ноя. 13, 2024
Язык: Английский
Процитировано
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