Silver and Copper‐Catalyzed Cycloaddition Reactions of Isocyanide Esters

Abstract Owing to multiple reactive sites, such as an acidic α‐carbon and an isocyano group, isocyanide esters can successfully participate in the synthesis of various five‐ and six‐membered N ‐heterocycles through the cycloaddition reactions under metal‐catalyzed systems. Considering the unique and versatile functionality of this synthon, in this review, we have highlighted silver and copper‐catalyzed cycloadditions of isocyanide esters over the last decade.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2024-10-11
DOI
https://doi.org/10.1002/adsc.202400994
Citations
5
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
1.25
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article

Silver and Copper‐Catalyzed Cycloaddition Reactions of Isocyanide Esters

Fatemeh Doraghi, Navid Dastyafteh, Milad Noori, Farzad Gilaninezhad et al.
5 citations
Advanced Synthesis & Catalysis
Catalytic Alkyne Reactions
1.25
article

Silver and Copper‐Catalyzed Cycloaddition Reactions of Isocyanide Esters

Fatemeh Doraghi, Navid Dastyafteh, Milad Noori, Farzad Gilaninezhad, Mohammad Mahdavi, Negar Mehdi zadeh Darban, Parsa Baghershahi
article en
5 citations

Abstract

Abstract Owing to multiple reactive sites, such as an acidic α‐carbon and an isocyano group, isocyanide esters can successfully participate in the synthesis of various five‐ and six‐membered N ‐heterocycles through the cycloaddition reactions under metal‐catalyzed systems. Considering the unique and versatile functionality of this synthon, in this review, we have highlighted silver and copper‐catalyzed cycloadditions of isocyanide esters over the last decade.

Advanced Synthesis & CatalysisVol. 367(4)
University of Tehran (IR), Iran University of Science and Technology (IR), Tehran University of Medical Sciences (IR), K. N. Toosi University of Technology (IR)
Openalex Percentile: Top 22%
Catalytic Alkyne Reactions
1.25
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