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European Journal of Organic Chemistry is a peer-reviewed journal published by Wiley, covering Catalytic C–H Functionalization Methods, Asymmetric Synthesis and Catalysis, Chemical Synthesis and Analysis.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." European Journal of Organic Chemistry 12 (3): 45–58.
Formats any DOI in European Journal of Organic Chemistry style. No sign-up. |
| Publishes research in | Catalytic C–H Functionalization Methods Asymmetric Synthesis and Catalysis Chemical Synthesis and Analysis Synthetic Organic Chemistry Methods Synthesis and Catalytic Reactions |
| ISSN | 1099-0690 |
| Citation impact (2-yr) | 2.38 |
| h-index | 184 |
| i10-index | 13,183 |
| Total citations | 479,571 |
| Article processing charge | $4,120 |
| Top institutions publishing here | Centre National de la Recherche Scientifique |
| Journal website | onlinelibrary.wiley.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Abstract The spiro[pyrrolidine‐3,3′‐oxindole] ring system is found at the core of a number of alkaloids, which possess significant biological activity and are interesting, challenging targets for chemical synthesis. In the present review, we report on the different strategies for the synthesis of the spiro[pyrrolidine‐3,3′‐oxindole] ring system in the context of recent synthesis of coerulescine, horsfiline,…
Abstract Cu I ‐catalyzed alkyne–azide cycloaddition provides 1,4‐disubstituted 1,2,3‐triazoles with such efficiency and scope that the transformation has been described as “click” chemistry. An overview of the mechanism of this remarkable reaction is presented as a means to explain the myriad of experimental results, particularly the various methods of catalyst generation, solvent and substrate effects,…
Abstract Recent progress in the field of asymmetric organocatalytic 1,4‐conjugate addition reactions, regarded as belonging among the more synthetically important carbon–carbon bond‐forming reactions, is described. The focus is on some recent advances in the following selected reactions: additions of various nucleophiles to α,β‐unsaturated cyclic and acyclic enals, enones, vinyl sulfones and nitro olefins, addition of…
Abstract Although the synthesis of β‐lactams by means of tethered Ugi reactions has been known since the early 1960s, the 1995 report from Ugi’s group could be regarded as a turning point in the development of novel multicomponent reactions (MCRs) for heterocycle syntheses. Indeed, the number of articles describing isocyanide‐based multicomponent syntheses of heterocycles has…
The asymmetric conjugate addition of various carbon and heteroatom nucleophiles to nitroalkenes as a tool for the construction of highly functionalized synthetic building blocks is presented. Diastereoselective, substrate-controlled 1,4-additions are also included. Besides auxiliary controlled asymmetric Michael additions, external asymmetric versions employing enantiopure additives, addition-elimination processes with enantiopure leaving groups, and catalytic asymmetric syntheses are…
