Synthesis of new azido porphyrins and their reactivity in copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition reaction with alkynes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Cu I ‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective
2. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
3. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
4. Synthesis and Versatile Reactions of β-Azidotetraarylporphyrins
5. Efficient Synthesis of Monoacyl Dipyrromethanes and Their Use in the Preparation of Sterically Unhindered trans-Porphyrins
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2. Meso-Formyl, Vinyl, and Ethynyl Porphyrins—Multipotent Synthons for Obtaining a Diverse Array of Functional Derivatives;Molecules;2023-07-31
3. CuAAC-inspired synthesis of 1,2,3-triazole-bridged porphyrin conjugates: an overview;Beilstein Journal of Organic Chemistry;2023-03-22
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5. Copper(II) phthalocyanine as an efficient and versatile catalyst for click reactions at room temperature;Journal of the Iranian Chemical Society;2022-06-29
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