David Martin

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Université Grenoble Alpes

France

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Recent Grants

Grant: Close

Aldehydes as metal surrogates for reductions – AldyRed

Open Date: 2020-12-20

Close Date: 2024-12-19

Grant: Close

Upgrading Cyanines dyes: Non-Kekulé ketocyanines and related patterns

Open Date: 2020-08-01

Close Date: 2022-07-31

Grant: Close

From elusive non-Kekulé species to bottle-able functional molecular bricks – NO-KEKULE-RULES

Open Date: 2017-05-20

Close Date: 2018-11-19

Grant: Close

Hydrogen atom donors and cooperative ligands stemming from oxyallyl frameworks – HALIGO

Open Date: 2014-09-20

Close Date: 2018-09-19

Articles (13)

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2024

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2024

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2024

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2024

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2023

Amides are redox stereoelectronic chameleons, which can act as strong acceptors and allow for the design of air-stable radicals.

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2023

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2023

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2023

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2022

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2021

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2020

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2020

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2020

Collaborators (4)

Tahar ayad

ASSOCIATE PROFESSOR

ENSAM

FRANCE

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Rodolphe Jazzar

University of California, San Diego

UNITED STATES

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David VIRIEUX

Professor

Ecole Nationale Supérieure de Chimie de Montpellier

FRANCE

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Jesse Peltier

Assistant Professor

Northeastern University

UNITED STATES

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David Martin

Research Interests

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Recent Grants

Articles (13)

Benchmarking Methanophosphocines as Versatile P<sup>III</sup>/P<sup>V</sup> Redox Organocatalysts

Boosting <i>N</i>-Heterocyclic Carbene Radical Organocatalysis with Nickel Chemistry: A Rational Mechanistic Study-Based Approach

Improved Protocols for the Synthesis of Precursors of Thiazol-2-ylidene N-Heterocyclic Carbenes

A simple N-heterocyclic carbene for the catalytic up-conversion of aldehydes into stoichiometric super electron donors

Beyond the Limits of Atropochirality: Design of Highly Conformationally Restrained Biaryls with Bridgehead Phosphine Oxide

An air-stable radical with a redox-chameleonic amide

On the Redox Properties of the Dimers of Thiazol-2-ylidenes That Are Relevant for Radical Catalysis

Bending Enamine Patterns of Stabilized Pentalenes into “Polymethine Ylides”

The curious case of a sterically crowded Stenhouse salt

Critical Assessment of the Reducing Ability of Breslow‐type Derivatives and Implications for Carbene‐Catalyzed Radical Reactions**

Absolute Templating of M(111) Cluster Surrogates by Galvanic Exchange.

Air‐Stable Oxyallyl Patterns and a Switchable N‐Heterocyclic Carbene

Air‐Stable Oxyallyl Patterns and a Switchable N‐Heterocyclic Carbene

Collaborators (4)

Tahar ayad

Rodolphe Jazzar

David VIRIEUX

Jesse Peltier

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