D-Index & Metrics Best Publications
Chemistry
Switzerland
2023

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 71 Citations 17,343 290 World Ranking 3299 National Ranking 89

Research.com Recognitions

Awards & Achievements

2023 - Research.com Chemistry in Switzerland Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Catalysis
  • Enzyme

His primary areas of study are Organic chemistry, Catalysis, Carbene, Enantioselective synthesis and Combinatorial chemistry. His Catalysis research includes themes of Benzoin and Redox. His Carbene research incorporates themes from Stereoisomerism, Organocatalysis, Annulation and Bicyclic molecule, Stereochemistry.

His Enantioselective synthesis research is multidisciplinary, incorporating perspectives in Diels alder, Claisen rearrangement, Aqueous solution and Regioselectivity. His Combinatorial chemistry research integrates issues from Peptide bond, Bond formation, Nanotechnology and Organic Chemistry Phenomena. The Amide study combines topics in areas such as Chemical ligation, Peptide, Bioconjugation and Drug discovery.

His most cited work include:

  • Rethinking amide bond synthesis (993 citations)
  • N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates: γ-Butyrolactones by Direct Annulations of Enals and Aldehydes (530 citations)
  • On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums (375 citations)

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

His primary areas of investigation include Organic chemistry, Combinatorial chemistry, Catalysis, Reagent and Stereochemistry. His studies deal with areas such as Protein biosynthesis, Potassium, Peptide bond, Peptide and Chemical synthesis as well as Combinatorial chemistry. His Peptide study incorporates themes from Amino acid, Hydroxylamine and Amide.

His research on Catalysis frequently links to adjacent areas such as Redox. His studies in Reagent integrate themes in fields like Stoichiometry, Tin and Amine gas treating. The various areas that Jeffrey W. Bode examines in his Carbene study include Salt and Electrophile.

He most often published in these fields:

  • Organic chemistry (35.83%)
  • Combinatorial chemistry (39.57%)
  • Catalysis (28.07%)

What were the highlights of his more recent work (between 2016-2021)?

  • Combinatorial chemistry (39.57%)
  • Peptide (24.06%)
  • Stereochemistry (23.80%)

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

His scientific interests lie mostly in Combinatorial chemistry, Peptide, Stereochemistry, Hydroxylamine and Reagent. His work deals with themes such as Protein biosynthesis, Potassium, Enantiopure drug and Peptide synthesis, which intersect with Combinatorial chemistry. His Potassium research is included under the broader classification of Organic chemistry.

His studies examine the connections between Stereochemistry and genetics, as well as such issues in Peptide bond, with regards to Threonine. His Hydroxylamine study integrates concerns from other disciplines, such as Chemical synthesis and Amide. His work carried out in the field of Reagent brings together such families of science as Iminium, Catalysis, Tin and Amine gas treating.

Between 2016 and 2021, his most popular works were:

  • Chemical Protein Synthesis with the α-Ketoacid-Hydroxylamine Ligation. (51 citations)
  • Chemoselective Acylation of Primary Amines and Amides with Potassium Acyltrifluoroborates under Acidic Conditions (42 citations)
  • Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate. (30 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

Rethinking amide bond synthesis

Vijaya R. Pattabiraman;Jeffrey W. Bode.
Nature (2011)

1617 Citations

N-Heterocyclic Carbene-Catalyzed Generation of Homoenolates: γ-Butyrolactones by Direct Annulations of Enals and Aldehydes

Stephanie S. Sohn;Evelyn L. Rosen;Jeffrey W. Bode.
Journal of the American Chemical Society (2004)

790 Citations

On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums

Jessada Mahatthananchai;Jeffrey W. Bode.
Accounts of Chemical Research (2014)

563 Citations

Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes.

Ming He;Justin R Struble;Jeffrey W Bode.
Journal of the American Chemical Society (2006)

561 Citations

Chemoselective Amide Ligations by Decarboxylative Condensations of N-Alkylhydroxylamines and α-Ketoacids†

Jeffrey W. Bode;Ryan M. Fox;Kyle D. Baucom.
Angewandte Chemie (2006)

428 Citations

N-Heterocyclic Carbene-Catalyzed Redox Amidations of α-Functionalized Aldehydes with Amines

Jeffrey W Bode;Stephanie S Sohn.
Journal of the American Chemical Society (2007)

365 Citations

Catalytic generation of activated carboxylates: Direct, stereoselective synthesis of β-hydroxyesters from epoxyaldehydes

Kenneth Yu-Kin Chow;Jeffrey W. Bode.
Journal of the American Chemical Society (2004)

365 Citations

Catalytic Selective Synthesis

Jessada Mahatthananchai;Aaron M. Dumas;Jeffrey W. Bode.
Angewandte Chemie (2012)

362 Citations

Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene Diels-Alder reactions with low catalyst loadings.

Ming He;Gerson J. Uc;Jeffrey W. Bode.
Journal of the American Chemical Society (2006)

344 Citations

An Enantioselective Claisen Rearrangement Catalyzed by N-Heterocyclic Carbenes

Juthanat Kaeobamrung;Jessada Mahatthananchai;Pinguan Zheng;Jeffrey W. Bode.
Journal of the American Chemical Society (2010)

336 Citations

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