D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 58 Citations 10,795 305 World Ranking 5701 National Ranking 208

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

Stereochemistry, Crystallography, Medicinal chemistry, Crystal structure and Reactivity are his primary areas of study. His biological study spans a wide range of topics, including Ligand, Sulfur, Deprotonation and Nucleophile. His studies deal with areas such as Inorganic chemistry, Ion, Molecule and Delocalized electron as well as Crystallography.

His Medicinal chemistry research includes themes of Organic chemistry, Ring and Alkyl. His Crystal structure study integrates concerns from other disciplines, such as Samarium, Steric effects, X-ray crystallography, Methylene and Divalent. He has researched Reactivity in several fields, including Pyridine, Pincer movement, Homoleptic, Carbene and Double bond.

His most cited work include:

  • Phosphine gold(I) bis-(trifluoromethanesulfonyl)imidate complexes as new highly efficient and air-stable catalysts for the cycloisomerization of enynes. (512 citations)
  • Asymmetric Synthesis and Highly Diastereoselective ortho-Lithiation of Ferrocenyl Sulfoxides. Application to the Synthesis of Ferrocenyl Derivatives with Planar Chirality (136 citations)
  • An Ni4 Single‐Molecule Magnet: Synthesis, Structure and Low‐Temperature Magnetic Behavior (127 citations)

What are the main themes of his work throughout his whole career to date?

His scientific interests lie mostly in Stereochemistry, Crystallography, Crystal structure, Medicinal chemistry and Organic chemistry. His Stereochemistry study also includes fields such as

  • Ligand together with Palladium,
  • Rhodium and related Iridium. As a part of the same scientific family, Louis Ricard mostly works in the field of Crystallography, focusing on Inorganic chemistry and, on occasion, Metal.

His Crystal structure research includes elements of Phosphole, Cyclopentadienyl complex, Phosphorus, X-ray crystallography and Nuclear magnetic resonance spectroscopy. His Medicinal chemistry study combines topics in areas such as Yield, Photochemistry, Cationic polymerization and Catalysis. As part of his studies on Organic chemistry, Louis Ricard often connects relevant subjects like Polymer chemistry.

He most often published in these fields:

  • Stereochemistry (33.85%)
  • Crystallography (33.33%)
  • Crystal structure (32.04%)

What were the highlights of his more recent work (between 2004-2019)?

  • Stereochemistry (33.85%)
  • Crystallography (33.33%)
  • Medicinal chemistry (21.96%)

In recent papers he was focusing on the following fields of study:

Louis Ricard mainly focuses on Stereochemistry, Crystallography, Medicinal chemistry, Crystal structure and Ligand. Louis Ricard combines subjects such as Chelation, Ferrocene, Enantiopure drug, Reactivity and Stereoselectivity with his study of Stereochemistry. His study focuses on the intersection of Crystallography and fields such as Inorganic chemistry with connections in the field of Phosphorus.

The study incorporates disciplines such as Cationic polymerization, Organic chemistry, Catalysis, Regioselectivity and Aryl in addition to Medicinal chemistry. His Crystal structure research incorporates themes from Phosphonate, Cyclopentadienyl complex, Solvation, Pincer movement and Deprotonation. His Ligand research is multidisciplinary, incorporating elements of Derivative, Yield, Polymer chemistry and Palladium.

Between 2004 and 2019, his most popular works were:

  • Phosphine gold(I) bis-(trifluoromethanesulfonyl)imidate complexes as new highly efficient and air-stable catalysts for the cycloisomerization of enynes. (512 citations)
  • New mono- and bis-carbene samarium complexes: synthesis, X-ray crystal structures and reactivity. (97 citations)
  • Very Large Ising‐Type Magnetic Anisotropy in a Mononuclear NiII Complex (89 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Catalysis
  • Alkene

Louis Ricard mostly deals with Stereochemistry, Medicinal chemistry, Ligand, Reactivity and Crystallography. His Stereochemistry research incorporates elements of Trifluoromethyl, Oxidative cyclization, Polymer chemistry and Chiral auxiliary. His Medicinal chemistry research is multidisciplinary, relying on both Denticity, Aryl, Alkyl and Phosphine.

His research on Ligand also deals with topics like

  • Palladium that intertwine with fields like Allylic rearrangement,
  • Catalysis, which have a strong connection to Combinatorial chemistry. His work deals with themes such as Pyridine, Crystal structure, Homoleptic, Carbene and Stereoselectivity, which intersect with Reactivity. His Crystallography study incorporates themes from Samarium, Delocalized electron, Electronic structure, HOMO/LUMO and Pentamethylcyclopentadiene.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Phosphine gold(I) bis-(trifluoromethanesulfonyl)imidate complexes as new highly efficient and air-stable catalysts for the cycloisomerization of enynes.

Nicolas Mézailles;Louis Ricard;Fabien Gagosz.
Organic Letters (2005)

796 Citations

Asymmetric Synthesis and Highly Diastereoselective ortho-Lithiation of Ferrocenyl Sulfoxides. Application to the Synthesis of Ferrocenyl Derivatives with Planar Chirality

François Rebière;Olivier Riant;Louis Ricard;Henri B. Kagan.
Angewandte Chemie (1993)

206 Citations

An Ni4 Single‐Molecule Magnet: Synthesis, Structure and Low‐Temperature Magnetic Behavior

María Moragues-Cánovas;Madeleine Helliwell;Louis Ricard;Éric Rivière.
European Journal of Inorganic Chemistry (2004)

193 Citations

Complexes of functional phosphines. 4. Coordination properties of (diphenylphosphino)acetonitrile, ethyl (diphenylphosphino)acetate and corresponding carbanions. Characterization of a new facile reversible carbon dioxide insertion into palladium(II) complexes

Pierre Braunstein;Dominique Matt;Yves Dusausoy;Jean Fischer.
Journal of the American Chemical Society (1981)

170 Citations

A general route to enantiomerically pure sulfoxides from a chiral sulfite

F. Rebiere;O. Samuel;L. Ricard;H. B. Kagan.
Journal of Organic Chemistry (1991)

162 Citations

The structure of the heteropolytungstate (NH4)17Na NaW21Sb9O86-14H2O. An inorganic crypate.

Jean Fischer;Louis Ricard;Raymond Weiss.
Journal of the American Chemical Society (1976)

145 Citations

New mono- and bis-carbene samarium complexes: synthesis, X-ray crystal structures and reactivity.

Thibault Cantat;Florian Jaroschik;François Nief;Louis Ricard.
Chemical Communications (2005)

145 Citations

Mechanism of the Stille reaction catalyzed by palladium ligated to arsine ligand: PhPdI(AsPh3)(DMF) is the species reacting with vinylstannane in DMF.

Christian Amatore;Ali A. Bahsoun;Anny Jutand;Gilbert Meyer.
Journal of the American Chemical Society (2003)

139 Citations

BIPNOR: A New, Efficient Bisphosphine Having Two Chiral, Nonracemizable, Bridgehead Phosphorus Centers for Use in Asymmetric Catalysis

Frédéric Robin;François Mercier;Louis Ricard;François Mathey.
Chemistry: A European Journal (1997)

117 Citations

Silacalix-[n]-phosphaarenes: Macrocyclic Ligands Based on Dicoordinate Phosphorus Centers

Narcis Avarvari;Nicolas Mézailles;Louis Ricard;Pascal Le Floch.
Science (1998)

111 Citations

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