Author
Nadia Pastori
Other affiliations: Polimeri Europa, Instituto Politécnico Nacional
Bio: Nadia Pastori is an academic researcher from Polytechnic University of Milan. The author has contributed to research in topics: Radical & Ketyl. The author has an hindex of 11, co-authored 28 publications receiving 426 citations. Previous affiliations of Nadia Pastori include Polimeri Europa & Instituto Politécnico Nacional.
Topics: Radical, Ketyl, Aryl, Catalysis, Aqueous solution
Papers
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TL;DR: In this paper, the authors used catalytic amount of Ti(IV) chloride in MeOH in the presence of NH3 or Et3N to achieve the acetalization of aliphatic and aromatic aldehydes.
78 citations
TL;DR: The use of TiCl4 as a catalyst for the acetalisation, at room temperature, of carbonyl compounds is reported in this paper, where mechanistic features are accounted for.
75 citations
TL;DR: An overview of some of the most significant contributions in the field, that covers the last decade, emphasizing the key role played by titanium salts in the promotion of selective reactions aimed at the synthesis of multifunctional organic compounds.
Abstract: Titanium complexes have been widely used as catalysts for C‑C bond-forming processes via free-radical routes. Herein we provide an overview of some of the most significant contributions in the field, that covers the last decade, emphasizing the key role played by titanium salts in the promotion of selective reactions aimed at the synthesis of multifunctional organic compounds, including nucleophilic radical additions to imines, pinacol and coupling reactions, ring opening of epoxides and living polymerization.
50 citations
TL;DR: In this article, the role of the metal ion in aminomethylation of ethers is discussed and amino-alkylation is also considered and the role role of metal ion is discussed.
38 citations
TL;DR: An amine, an aldehyde, and methanol can be readily assembled in one pot under very mild conditions through a free-radical multicomponent reaction by using an aqueous acidic TiCl3/t-BuOOH system to afford 1,2-amino alcohols in fair to excellent yields.
37 citations
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TL;DR: A comprehensive overview on first row transition metal catalysts for C-H activation until summer 2018 is provided.
Abstract: C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with notable applications to material sciences, crop protection, drug discovery, and pharmaceutical industries, among others. Despite major advances, the vast majority of these C–H functionalizations required precious 4d or 5d transition metal catalysts. Given the cost-effective and sustainable nature of earth-abundant first row transition metals, the development of less toxic, inexpensive 3d metal catalysts for C–H activation has gained considerable recent momentum as a significantly more environmentally-benign and economically-attractive alternative. Herein, we provide a comprehensive overview on first row transition metal catalysts for C–H activation until summer 2018.
1,417 citations
TL;DR: Seven kinds of sp(3)α-C-H activation/C-C formation reactions of alcohols and ethers have been reviewed in this tutorial review, from the viewpoint of both methodology and synthetic application, towards the efficiency, chemo-, regio- and stereoselectivity, catalytic system, substrate scope and mechanistic study.
Abstract: Seven kinds of sp3 α-C–H activation/C–C formation reactions of alcohols and ethers have been reviewed in this tutorial review, from the viewpoint of both methodology and synthetic application, towards the efficiency, chemo-, regio- and stereoselectivity, catalytic system, substrate scope and mechanistic study. Section 2 describes radical-mediated α-C–H activation and addition/elimination of ethers with unsaturated (CC and CC) species. Sections 3–8 discuss the α-C–H activation and additions of alcohols and/or ethers with unsaturated (CC, CC, CO and CN) compounds, which involve the key processes of radical mediation, carbenoid insertion, 1,5-H-migration, oxidative dehydrogenation coupling, transfer hydrogenative coupling, and metal-mediated CC insertion into the C–H bond.
413 citations
TL;DR: The mechanisms and the applications in organic synthesis, materials, supramolecular, and polymer synthesis of most organic reactions mediated by single electron transfer are discussed, even though both biology and radical chemistry rely extensively on one-electron transfer processes.
Abstract: The article discusses the mechanisms and the applications in organic synthesis, materials, supramolecular, and polymer synthesis of most organic reactions mediated by single electron transfer. Each reaction or class of reactions will be discussed by starting with the original discovery publication, followed by a summary of all or most review articles published in the field, and a discussion of the mechanism(s) and of the most important methodologic and synthetic developments since the most recent review was published. The mechanisms of most organic reactions are considered to proceed by two-electron transfer pathways, even though both biology and radical chemistry rely extensively on one-electron transfer processes. Radicals generated by homolytic cleavage at high temperature were traditionally employed in the industrial production of polymers and to a lesser extent in the synthesis of organic molecules.
320 citations
TL;DR: Transition-metal-catalyzed C H functionalization for the atomand step-economical synthesis of functional molecules has attracted tremendous efforts in both academia and industry, with high efficiency, low cost, and minimal environmental impact.
Abstract: Transition-metal-catalyzed C H functionalization for the atomand step-economical synthesis of functional molecules has attracted tremendous efforts in both academia and industry. The advantages of this method are the high efficiency, low cost, and minimal environmental impact. Heteroatom-containing molecules are abundant in natural products, pharmaceuticals, and materials. It is highly desirable to synthesize these molecules and their derivatives by direct C H functionalization. Metal carbene insertion into a C H bond adjacent to an oxygen atom presents an efficient synthetic approach to ether derivatives (Scheme 1, Meth-
264 citations
TL;DR: The title reaction proceeds in the absence of transition metal catalysts, is operationally simple and tolerates a wide variety of functional groups like cyano, amide, aromatic halide, ether, ketone groups and C-C double bonds.
Abstract: Title reaction proceeds in the absence of transition metal catalysts, is operationally simple and tolerates a wide variety of functional groups like cyano, amide, aromatic halide, ether, ketone groups and C—C double bonds.
253 citations