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 46 Citations 6,508 136 World Ranking 10380 National Ranking 2942

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Alkene

His primary areas of investigation include Organic chemistry, Trifluoromethyl, Trifluoromethylation, Reagent and Fluorine. His is doing research in Electrophile, Catalysis, Tetrakisethylene and Ethylene, both of which are found in Organic chemistry. His studies deal with areas such as Thio- and Medicinal chemistry as well as Trifluoromethyl.

He has researched Trifluoromethylation in several fields, including Inorganic chemistry, Potassium, Nucleophile and Enantioselective synthesis. Many of his studies involve connections with topics such as Combinatorial chemistry and Reagent. His work in Fluorine tackles topics such as Molecule which are related to areas like Indole test and Yield.

His most cited work include:

  • Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept (266 citations)
  • Formation of C-SCF3 bonds through direct trifluoromethylthiolation. (193 citations)
  • Electrophilic trifluoromethanesulfanylation of organometallic species with trifluoromethanesulfanamides. (182 citations)

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

Organic chemistry, Reagent, Trifluoromethyl, Combinatorial chemistry and Fluorine are his primary areas of study. All of his Organic chemistry and Trifluoromethylation, Reactivity, Trimethylsilane, Yield and Diels alder investigations are sub-components of the entire Organic chemistry study. His study in Reagent is interdisciplinary in nature, drawing from both Photochemistry, Electrophile, Molecule and Nucleophile.

The Nucleophile study combines topics in areas such as Potassium and Hemiaminal. His study looks at the relationship between Trifluoromethyl and fields such as Medicinal chemistry, as well as how they intersect with chemical problems. Thierry Billard has included themes like Catalysis and Selenium in his Fluorine study.

He most often published in these fields:

  • Organic chemistry (44.14%)
  • Reagent (27.93%)
  • Trifluoromethyl (21.17%)

What were the highlights of his more recent work (between 2015-2021)?

  • Reagent (27.93%)
  • Combinatorial chemistry (18.92%)
  • Organic chemistry (44.14%)

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

His primary scientific interests are in Reagent, Combinatorial chemistry, Organic chemistry, Fluorine and Trifluoromethyl. His work carried out in the field of Reagent brings together such families of science as Electrophile, Catalysis, Medicinal chemistry, Reactivity and Molecule. His work deals with themes such as Substituent and Organic molecules, which intersect with Electrophile.

His research in Molecule intersects with topics in Electrophilic aromatic substitution and Electrophilic addition. His work focuses on many connections between Combinatorial chemistry and other disciplines, such as Moiety, that overlap with his field of interest in Group. His Trifluoromethyl research includes themes of Luminescence, Photochemistry, Reaction conditions and Bond formation.

Between 2015 and 2021, his most popular works were:

  • Synthetic Approaches to Trifluoromethoxy-Substituted Compounds (100 citations)
  • Benzyltrifluoromethyl (or Fluoroalkyl) Selenide: Reagent for Electrophilic Trifluoromethyl (or Fluoroalkyl) Selenolation. (43 citations)
  • Direct Electrophilic (Benzenesulfonyl)Difluoromethylthiolation with a Shelf-Stable Reagent. (42 citations)

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

Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept

Fabien Toulgoat;Sébastien Alazet;Thierry Billard.
European Journal of Organic Chemistry (2014)

450 Citations

Formation of C-SCF3 bonds through direct trifluoromethylthiolation.

Anis Tlili;Thierry Billard.
Angewandte Chemie (2013)

308 Citations

Trifluoromethanesulfanylamides as Easy‐to‐Handle Equivalents of the Trifluoromethanesulfanyl Cation (CF3S+): Reaction with Alkenes and Alkynes

Aurélien Ferry;Thierry Billard;Bernard R. Langlois;Eric Bacqué.
Angewandte Chemie (2009)

255 Citations

Preparation of trifluoromethyl sulfides or selenides from trifluoromethyl trimethylsilane and thiocyanates or selenocyanates

Thierry Billard;Sylvie Large;Bernard R Langlois.
Tetrahedron Letters (1997)

228 Citations

Electrophilic trifluoromethanesulfanylation of organometallic species with trifluoromethanesulfanamides.

François Baert;Julie Colomb;Thierry Billard.
Angewandte Chemie (2012)

219 Citations

Synthesis of trifluoromethanesulfinamidines and -sulfanylamides.

Aurélien Ferry;Thierry Billard;Bernard R. Langlois;Eric Bacqué.
Journal of Organic Chemistry (2008)

216 Citations

Synthetic Approaches to Trifluoromethoxy-Substituted Compounds.

Anis Tlili;Fabien Toulgoat;Fabien Toulgoat;Thierry Billard.
Angewandte Chemie (2016)

201 Citations

Some Recent Results in Nucleophilic Trifluoromethylation and Introduction of Fluorinated Moieties

Bernard R. Langlois;Thierry Billard.
Synthesis (2003)

194 Citations

Electrophilic trifluoromethanesulfanylation of indole derivatives

Aurélien Ferry;Thierry Billard;Eric Bacqué;Bernard R. Langlois.
Journal of Fluorine Chemistry (2012)

168 Citations

A new simple access to trifluoromethyl thioethers or selenoethers from trifluoromethyl trimethylsilane and disulfides or diselenides

Thierry Billard;Bernard R Langlois.
Tetrahedron Letters (1996)

156 Citations

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