Progress in heterocyclic chemistry, Journal Year: 2023, Volume and Issue: unknown, P. 281 - 332
Published: Jan. 1, 2023
Language: Английский
Progress in heterocyclic chemistry, Journal Year: 2023, Volume and Issue: unknown, P. 281 - 332
Published: Jan. 1, 2023
Language: Английский
ACS Omega, Journal Year: 2022, Volume and Issue: 7(42), P. 36945 - 36987
Published: Oct. 10, 2022
1,2,3-Triazole scaffolds are not obtained in nature, but they still intensely investigated by synthetic chemists various fields due to their excellent properties and green routes. This review will provide a library of all routes used the past 21 years synthesize 1,2,3-triazoles derivatives using metal catalysts (such as Cu, Ni, Ru, Ir, Rh, Pd, Au, Ag, Zn, Sm), organocatalysts, metal-free well solvent- catalyst-free neat syntheses, along with mechanistic cycles, recyclability studies, solvent systems, reaction condition effects on regioselectivity. Constant developments indicate that help lead future organic synthesis useful for creating molecular libraries functionalized 1,2,3-triazoles.
Language: Английский
Citations
80European Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 27(11)
Published: Jan. 29, 2024
Abstract 2H ‐arizines are important three‐membered heterocycles in organic chemistry. Recently, many advances the synthesis and functionalization of have been reported. Neber rearrangement, isomerization isoxazole, oxidation enamine, C−H bond activation, decomposition vinyl azide, alkyne, multi‐step developed for efficient assembly ‐azirines. As versatile highly strained unsaturated heterocycles, ‐azirines can be used as distinctive building blocks towards significant functional groups, attracted extensive attention fabrication numerous heterocycles. Recent studies focused on [3+n] ring‐expansion reactions, nucleophilic addition C=N double or continuous followed by cyclization, ring‐opening to acyclic compounds, substitution sp 3 ‐C−H One most critical challenges is seeking a selective opening specific three bonds azirine circle, some what achieved basis metal catalyst, photocatalysis, combination catalyst photocatalysis. In this review, recent involving reactivity accompanied with breakthroughs summarized. The review mainly covers period from 2019 2023.
Language: Английский
Citations
12ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(15), P. 11646 - 11656
Published: July 22, 2024
Language: Английский
Citations
7The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: April 18, 2025
The 1,2,3-triazole scaffolds are an important class of biologically privileged heterocyclic compounds with several key applications in chemistry, biology, medicine, agriculture, and material science. "postclick" functionalization 1,2,3-triazoles may emerge as a promising tactic for the construction molecular architectures therapeutics is considered to be growing area investigation. This interest extends beyond regioselective Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) method that involves trapping Cu(I)-triazole suitable precursors. In this Perspective, we highlight impact postclick strategies organic synthesis required late-stage hope emerging concept provide ample opportunities modern notable medicinal materials
Language: Английский
Citations
1Tetrahedron Letters, Journal Year: 2025, Volume and Issue: unknown, P. 155661 - 155661
Published: May 1, 2025
Language: Английский
Citations
0Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: 30(20)
Published: Feb. 26, 2024
Abstract The particular and unique mechanism of the copper‐catalyzed reaction between azides alkynes (CuAAC) has not only allowed for efficient synthesis 1,2,3‐trisubstituted 1,4‐triazoles in excellent yields under mild conditions, becoming quintessential click reaction, but it also enabled straightforward formation a metallocycle intermediate, copper triazolyl. This, suitable conditions able to suppress its protonolysis, can be used either creation new bicyclic triazolyl structures or generation novel three four‐component reactions. aim this review is rationalize unify all these transformations, which are collectively referred as “interrupted reactions”.
Language: Английский
Citations
3Organic Letters, Journal Year: 2024, Volume and Issue: 26(41), P. 8848 - 8853
Published: Oct. 8, 2024
A N-heterocyclic carbene-catalyzed (NHC) three-component reaction involving
Language: Английский
Citations
2Organic Letters, Journal Year: 2024, Volume and Issue: unknown
Published: Dec. 13, 2024
In this work, the annulation of acyl nitrene with alkynes is reported under photoredox/iron dual-catalysis for synthesis a series isoquninalin-2-ones. The reaction featured high regioselectivity and good generality. particular, resulting isoquinalin-2-ones could be structurally elaborated into several biologically interesting scaffolds. Mechanism investigation suggests that was ascribed to formal [4 + 2] cyclization. It believed represents an initial example preparing isoquinolin-1-ones from ferric peroxyl-catalyzed insertion.
Language: Английский
Citations
2Synthesis, Journal Year: 2023, Volume and Issue: 55(20), P. 3393 - 3401
Published: May 19, 2023
Abstract Copper-catalyzed coupling reaction involving N-phenoxyacetamides and 2H-azirines is described, in which N–O C–N bonds are broken restructured. This protocol provides an efficient strategy for the highly regioselective synthesis of racemic α-amino oxime ethers. In addition, this can be used to modify natural products gram-scale compatible.
Language: Английский
Citations
4Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(17), P. 3689 - 3694
Published: June 22, 2024
Abstract 2 H ‐Azirines are an important class of small‐ring heterocycle that have been employed as versatile synthetic building blocks. Herein, a one‐pot CuAAC/ring‐cleavage/[4+2]‐cycloaddition/rearrangement reaction sequence involving terminal ynones, sulfonyl azides and ‐azirines is reported leads to 2‐aminopyridine derivatives. In the first step, highly reactive N ‐sulfonyl α ‐acylketenimines generated, via CuAAC/ring‐cleavage process, from ynones these undergo inverse electron‐demand Diels–Alder cycloaddition reactions with form (isolable) 1,3‐oxazines themselves base‐promoted ring‐cleavage rearrangement afford title compounds.
Language: Английский
Citations
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