N. Mateu

发表

Synthesis of Structurally Diverse N‐Substituted Quaternary‐Carbon‐Containing Small Molecules from α,α‐Disubstituted Propargyl Amino Esters

Andreas Bender, David R Spring, Leen Kalash, 2018, Chemistry.

8-Iodonaphthalene-1-carbaldehyde: A Versatile Building Block for Diversity-Oriented Synthesis.

S. Fustero, N. Mateu, Raquel Román, 2016, Organic letters.

Synthesis and SAR of novel GPR39 Agonists and Positive Allosteric Modulators

Lewis H. Mervin, Justin J. W. Powell, R. Bürli, 2022, Bioorganic & Medicinal Chemistry Letters.

Synthesis of a new fluorinated oxazolidinone and its reactivity as a chiral auxiliary in Aldol reactions

Paula Bello, S. Fustero, N. Mateu, 2007 .

Development of a Novel Cell-Permeable Protein–Protein Interaction Inhibitor for the Polo-box Domain of Polo-like Kinase 1

D. Spring, G. McKenzie, A. Venkitaraman, 2019, ACS omega.

Base-dependent stereodivergent intramolecular aza-Michael reaction: asymmetric synthesis of 1,3-disubstituted isoindolines.

S. Fustero, Elsa Rodríguez, N. Mateu, 2013, Chemistry.

Asymmetric allylation/ring closing metathesis: one-pot synthesis of benzo-fused cyclic homoallylic amines. Application to the formal synthesis of Sertraline derivatives.

S. Fustero, Elsa Rodríguez, N. Mateu, 2013, Organic letters.

Stereoselective access to fluorinated and non-fluorinated quaternary piperidines: synthesis of pipecolic acid and iminosugar derivatives.

J. L. Aceña, S. Fustero, Javier Miró, 2012, Chemistry.

Diastereoselective intramolecular additions of allyl- and propargylsilanes to iminium ions: synthesis of cyclic and bicyclic quaternary amino acids.

J. L. Aceña, S. Fustero, N. Mateu, 2010, Organic letters.

Vinyl Fluorides: Competent Olefinic Counterparts in the Intramolecular Pauson-Khand Reaction.

M. Medio‐Simón, S. Fustero, N. Mateu, 2019, Organic letters.

Diastereoselective synthesis of 2-phenyl-3-(trifluoromethyl)piperazines as building blocks for drug discovery.

Ó. Delgado, Michiel Van Gool, María Sánchez-Roselló, 2014, The Journal of organic chemistry.

Asymmetric Synthesis of Fluorinated Monoterpenic Alkaloid Derivatives from Chiral Fluoroalkyl Aldimines via the Pauson‐Khand Reaction

A. Riera, M. Medio‐Simón, Jianlin Han, 2020 .

The Fluoro-Pauson-Khand Reaction in the Synthesis of Enantioenriched Nitrogenated Bicycles Bearing a Quaternary C-F Stereogenic Center.

M. Medio‐Simón, S. Fustero, N. Mateu, 2019, Organic letters.

Spirocycles as Rigidified sp3-Rich Scaffolds for a Fragment Collection.

D. Spring, S. L. Kidd, A. North, 2019, Organic letters.

Hydroxylated Rotenoids Selectively Inhibit the Proliferation of Prostate Cancer Cells.

D. A. Russell, D. Spring, D. Russell, 2020, Journal of natural products.

Copper-Catalyzed Regioselective Synthesis of (E)-β-Fluorovinyl Sulfones

S. Fustero, N. Mateu, Raquel Román, 2019, Molecules.

A Versatile Approach to CF3 -Containing 2-Pyrrolidones by Tandem Michael Addition-Cyclization: Exemplification in the Synthesis of Amidine Class BACE1 Inhibitors.

Ó. Delgado, Michiel Van Gool, G. Tresadern, 2015, Chemistry.

Demonstration of the utility of DOS-derived fragment libraries for rapid hit derivatisation in a multidirectional fashion†

Anthony R. Bradley, Christopher G. Dowson, Katherine E. McAuley, 2020, Chemical science.

Recent Applications of Diversity-Oriented Synthesis Toward Novel, 3-Dimensional Fragment Collections

David R. Spring, Sarah L. Kidd, Natalia Mateu, 2018, Front. Chem..

A Versatile Approach to CF3 -Containing 2-Pyrrolidones by Tandem Michael Addition-Cyclization: Exemplification in the Synthesis of Amidine Class BACE1 Inhibitors.

Ó. Delgado, Michiel Van Gool, G. Tresadern, 2015, Chemistry.

A Versatile Approach to CF3‐Containing 2‐Pyrrolidones by Tandem Michael Addition—Cyclization: Exemplification in the Synthesis of Amidine Class BACE1 Inhibitors.

Ó. Delgado, G. Tresadern, L. Pérez-Benito, 2016 .