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 53 Citations 6,476 195 World Ranking 9641 National Ranking 2771

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Enzyme
  • Catalysis

George A. O'Doherty spends much of his time researching Stereochemistry, Enantioselective synthesis, Dihydroxylation, Glycosylation and Catalysis. His Stereochemistry study incorporates themes from Furfural, Stereoisomerism, Alcohol, Ring and Stereoselectivity. George A. O'Doherty has included themes like Oligosaccharide and De novo synthesis in his Stereoselectivity study.

The concepts of his Enantioselective synthesis study are interwoven with issues in Ketone, Enantiomer and Palladium. His research integrates issues of Regioselectivity, Reductive amination, Trisaccharide, Talose and Luche reduction in his study of Dihydroxylation. His research in Glycosylation intersects with topics in Furan and Anomer.

His most cited work include:

  • De novo synthesis of oligosaccharides using a palladium-catalyzed glycosylation reaction. (137 citations)
  • A Palladium-Catalyzed Glycosylation Reaction: The de Novo Synthesis of Natural and Unnatural Glycosides (125 citations)
  • Synthesis of D- and L-deoxymannojirimycin via an asymmetric aminohydroxylation of vinylfuran. (107 citations)

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

George A. O'Doherty mostly deals with Stereochemistry, Enantioselective synthesis, Dihydroxylation, Glycosylation and Organic chemistry. His work deals with themes such as Stereoisomerism, Catalysis, Stereoselectivity and De novo synthesis, which intersect with Stereochemistry. His work in the fields of Catalysis, such as Palladium and Furfural, intersects with other areas such as Side chain.

His work in Enantioselective synthesis covers topics such as Regioselectivity which are related to areas like Sharpless asymmetric dihydroxylation. His Dihydroxylation study also includes fields such as

  • Ring which connect with Moiety and Ketone,
  • Luche reduction that connect with fields like Reductive amination. His work carried out in the field of Glycosylation brings together such families of science as Anomer and Monosaccharide.

He most often published in these fields:

  • Stereochemistry (62.33%)
  • Enantioselective synthesis (45.74%)
  • Dihydroxylation (25.56%)

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

  • Stereochemistry (62.33%)
  • Enantioselective synthesis (45.74%)
  • Biochemistry (9.87%)

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

His main research concerns Stereochemistry, Enantioselective synthesis, Biochemistry, Digitoxin and Total synthesis. George A. O'Doherty combines subjects such as Dihydroxylation, P90 Ribosomal S6 Kinase and Stereoisomerism with his study of Stereochemistry. The Stereoisomerism study combines topics in areas such as Diol and Chelation.

His Enantioselective synthesis research is multidisciplinary, incorporating elements of Natural product, Turn, Oligosaccharide synthesis and Regioselectivity. In the field of Biochemistry, his study on Glutamine and Glycosylation overlaps with subjects such as Conjugate, Side chain and Sex pheromone. Structure–activity relationship and Enantiomer is closely connected to Camptothecin in his research, which is encompassed under the umbrella topic of Diastereomer.

Between 2015 and 2021, his most popular works were:

  • Development of a RSK Inhibitor as a Novel Therapy for Triple-Negative Breast Cancer. (33 citations)
  • Autophagy‐Induced Apoptosis in Lung Cancer Cells by a Novel Digitoxin Analog (20 citations)
  • Nigericin decreases the viability of multidrug-resistant cancer cells and lung tumorspheres and potentiates the effects of cardiac glycosides. (17 citations)

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

  • Organic chemistry
  • Enzyme
  • Catalysis

The scientist’s investigation covers issues in Stereochemistry, Digitoxin, Biochemistry, Pharmacology and Cancer research. His Stereochemistry study combines topics from a wide range of disciplines, such as Structure–activity relationship, P90 Ribosomal S6 Kinase and Stereoselectivity. His Structure–activity relationship study combines topics in areas such as Lactone, Bufalin, Na+/K+-ATPase, Enzyme and IC50.

Biochemistry is a component of his Enantioselective synthesis and Glycosylation studies. His studies deal with areas such as Breast cancer and Triple-negative breast cancer as well as Pharmacology. His study in Apoptosis is interdisciplinary in nature, drawing from both Cell and Cell growth.

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

A Palladium-Catalyzed Glycosylation Reaction: The de Novo Synthesis of Natural and Unnatural Glycosides

Ravula Satheesh Babu;George A. O'doherty.
Journal of the American Chemical Society (2003)

206 Citations

De novo synthesis of oligosaccharides using a palladium-catalyzed glycosylation reaction.

Ravula Satheesh Babu;Maoquan Zhou;George A. O'Doherty.
Journal of the American Chemical Society (2004)

196 Citations

Synthesis of D- and L-deoxymannojirimycin via an asymmetric aminohydroxylation of vinylfuran.

Michael H. Haukaas;George A. O'Doherty.
Organic Letters (2001)

180 Citations

Asymmetric synthesis of allylic sulfones useful as asymmetric building blocks.

Barry M. Trost;Michael G. Organ;George A. O'Doherty.
Journal of the American Chemical Society (1995)

156 Citations

Syntheses of D- and L-Mannose, Gulose, and Talose via Diastereoselective and Enantioselective Dihydroxylation Reactions.

Harris Jm;Keranen;O'Doherty Ga.
Journal of Organic Chemistry (1999)

143 Citations

De novo approach to 2-deoxy-beta-glycosides: asymmetric syntheses of digoxose and digitoxin.

Maoquan Zhou;George A. O’Doherty.
Journal of Organic Chemistry (2007)

138 Citations

De Novo Asymmetric Synthesis of the Anthrax Tetrasaccharide by a Palladium‐Catalyzed Glycosylation Reaction

Haibing Guo;George A. O'Doherty.
Angewandte Chemie (2007)

138 Citations

Enantioselective Synthesis of 2-Deoxy- and 2,3-Dideoxyhexoses

Michael H. Haukaas;George A. O'Doherty.
Organic Letters (2002)

133 Citations

Syntheses of four D- and L-hexoses via diastereoselective and enantioselective dihydroxylation reactions.

Joel M. Harris;Mark D. Keränen;Hang Nguyen;Victor G. Young.
Carbohydrate Research (2000)

133 Citations

De novo asymmetric synthesis of D- and L-swainsonine.

Haibing Guo;George A. O'Doherty.
Organic Letters (2006)

125 Citations

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