Advances in organocatalysis of the Michael reaction by tertiary Phosphines
Author:
Affiliation:
1. A.M. Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
Funder
Kazan Federal University Strategic Academic Leadership Program
Publisher
Informa UK Limited
Subject
Process Chemistry and Technology,General Chemistry,Catalysis
Link
https://www.tandfonline.com/doi/pdf/10.1080/01614940.2023.2168352
Reference204 articles.
1. Quantitative analysis of ligand effects. Part 3. Separation of phosphorus(III) ligands into pure .sigma.-donors and .sigma.-donor/.pi.-acceptors. Comparison of basicity and .sigma.-donicity
2. Nucleophilic reactivity constants toward methyl iodide and trans-dichlorodi(pyridine)platinum(II)
3. A Theoretical Study of the Mechanism of Phosphine-Catalyzed Hydroalkoxylation of Methyl Vinyl Ketone
4. Mechanistic insights into N- or P-centered nucleophile promoted thiol–vinylsulfone Michael addition
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1. Michael addition of ethyl acetoacetate on dibenzylideneacetone derivatives: Synthesis, spectroscopy, antimicrobial and in silico studies;Journal of Molecular Structure;2025-02
2. Phosphine‐Catalyzed Synthesis and Cytotoxic Evaluation of Michael Adducts of the Sesquiterpene Lactone Arglabin;ChemMedChem;2024-04-14
3. α‐Umpolung/Michael Addition/Quaternization Tandem Reaction to provide α‐Imido‐β‐phosphonium Propanoates with Broad Spectrum of Biological Activity;Chemistry & Biodiversity;2024-02-21
4. Using the phospha-Michael reaction for making phosphonium phenolate zwitterions;Beilstein Journal of Organic Chemistry;2024-01-10
5. Stereoelectronic Effect in the Reaction of α-Methylene Lactones with Tertiary Phosphines and Its Application in Organocatalysis;The Journal of Organic Chemistry;2023-08-04
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