Author
Frédéric Lamaty
Other affiliations: Moscow State University, Purdue University, Aventis Pharma ...read more
Bio: Frédéric Lamaty is an academic researcher from University of Montpellier. The author has contributed to research in topics: Catalysis & Ethylene glycol. The author has an hindex of 38, co-authored 217 publications receiving 4687 citations. Previous affiliations of Frédéric Lamaty include Moscow State University & Purdue University.
Papers published on a yearly basis
Papers
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TL;DR: 1.5.1.
Abstract: 2.3.3. Fluorinated Imines 7 2.3.4. Arylimino Acetates 8 2.3.5. In Situ Generated Iminium Ions 8 2.4. -Substituted Michael Acceptors 8 2.5. Formation of Unexpected Products 10 2.5.1. Reaction with Cyclic Enones 11 2.5.2. Reaction with Vinyl Ketones 11 2.5.3. Reaction with Acrolein 12 2.5.4. Reaction with Activated Allenes and Alkynes 12 2.5.5. Reaction of Salicyl N-Tosylimines 12 3. Stereoselective Synthesis 13 3.1. Use of Chiral Aldehydes 13 3.2. Use of Chiral Bases 13 3.3. Use of Chiral Phosphines 16 3.4. Use of a Chiral Sulfide 18 3.5. Use of an Organocatalyst Derived from BINOL 18 3.6. Use of a Chiral Ligand Derived from Thiourea 18 3.7. Use of Chiral Ionic Liquids 18 4. Alternative Access Pathways to -Aminocarbonyl Compounds 18
483 citations
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TL;DR: A detailed overview on the synthesis of four-, five- and six-membered, saturated and unsaturated N -heterocyclic carbenes used in the preparation of their corresponding ruthenium complexes is presented both in solution and on solid support as mentioned in this paper.
187 citations
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TL;DR: Novel synthetic routes to various hydantoin structures, the advances brought to the classical methods in the aim of producing more sustainable and environmentally friendly procedures for the preparation of these biomolecules, and a critical comparison of the different synthetic approaches developed in the last twelve years are described.
Abstract: The review highlights the hydantoin syntheses presented from the point of view of the preparation methods. Novel synthetic routes to various hydantoin structures, the advances brought to the classical methods in the aim of producing more sustainable and environmentally friendly procedures for the preparation of these biomolecules, and a critical comparison of the different synthetic approaches developed in the last twelve years are also described. The review is composed of 95 schemes, 8 figures and 528 references for the last 12 years and includes the description of the hydantoin-based marketed drugs and clinical candidates.
136 citations
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TL;DR: The Zr-promoted bicyclization of 1,6-and 1,7-dienes can stereoselectively produce trans-zirconabicyclo[3.3.0] octanes and cis-Zircon-conabicycleclo [4.3] nonanes, respectively; these compounds can be readily converted into protonolysis, halogenolysis and carbonylation products as discussed by the authors.
126 citations
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TL;DR: In this paper, the authors describe an original methodology for peptide bond synthesis avoiding toxic solvents and reactants, which was successfully applied to the synthesis of Leu-enkephalin.
115 citations
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TL;DR: There is, I think, something ethereal about i —the square root of minus one, which seems an odd beast at that time—an intruder hovering on the edge of reality.
Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality.
Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …
33,785 citations
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28,685 citations
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TL;DR: s, or keywords if they used Heck-type chemistry in their syntheses, because it became one of basic tools of organic preparations, a natural way to make organic preparations.
Abstract: s, or keywords if they used Heck-type chemistry in their syntheses, because it became one of basic tools of organic preparations, a natural way to
3,373 citations
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TL;DR: This Review highlights recent applications of controlled microwave heating in modern organic synthesis, and discusses some of the underlying phenomena and issues involved.
Abstract: Although fire is now rarely used in synthetic chemistry, it was not until Robert Bunsen invented the burner in 1855 that the energy from this heat source could be applied to a reaction vessel in a focused manner. The Bunsen burner was later superseded by the isomantle, oil bath, or hot plate as a source for applying heat to a chemical reaction. In the past few years, heating and driving chemical reactions by microwave energy has been an increasingly popular theme in the scientific community. This nonclassical heating technique is slowly moving from a laboratory curiosity to an established technique that is heavily used in both academia and industry. The efficiency of "microwave flash heating" in dramatically reducing reaction times (from days and hours to minutes and seconds) is just one of the many advantages. This Review highlights recent applications of controlled microwave heating in modern organic synthesis, and discusses some of the underlying phenomena and issues involved.
3,044 citations
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2,594 citations