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29Barry M Trost Key Opinion Leader In [Barry M Trost is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]- 1Catalysis | 1Lactones | 1Alkenes | 1Alkynes | 1Stereoisomerism | 1Alkylation | 1Ruthenium | 2Palladium | 4Isomerism | 8Aldehydes | 11Macrolides | 17Organometallic Compounds | 41Molecular Structure | 94Ligands | 170Oxidation-Reduction | 238Anti-Bacterial Agents
Keywords (32) [keywords assigned to Barry M Trost articles by PubMed, the leading number and the color conveys importance]- 19Catalysis | 13Stereoisomerism | 8Ruthenium | 8Alkylation | 8Palladium | 7Alkynes | 5Alkenes | 5Molecular Structure | 4Lactones | 4Organometallic Compounds | 3Oxidation-Reduction | 3Ligands | 3Macrolides | 3Isomerism | 3Anti-Bacterial Agents | 3Aldehydes | 2Allyl Compounds | 2Molybdenum | 2Propanols | 2Zinc | 2Hydrocarbons, Cyclic | 2Kinetics | 2Heterocyclic Compounds | 1Benzoates | 1Polymers | 1Methane | 1Cholinesterase Inhibitors | 1Piperidines | 1Antineoplastic Agents | 1Ketones | 1Porifera | 1Naphthalenes
Other [context-specific ads]Barry M Trost Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Barry M Trost might be a good expert witness on these terms]- 30synthesis | 15asymmetric | 13allylic | 13reaction | 12alkylation | 9reactions | 8catalyzed | 7alkynes | 7total | 7alkenes | 6cycloisomerization | 6enantioselective | 6formation | 6ruthenium-catalyzed | 5efficient | 5trisubstituted | 5chiral | 5palladium-catalyzed | 5synthetic | 5coupling | 5mechanism | 4can | 4strategy | 4proposed | 4ligands | 4structure | 3using | 3alcohols | 3ligand | 3henry | 3bond | 3acid
- 12allylic alkylation | 8asymmetric allylic | 7total synthesis | 4enantioselective synthesis | 4trisubstituted alkenes | 3palladium-catalyzed asymmetric | 3henry reaction | 3efficient enantioselective | 3diastereoselective synthesis | 3oxidative cyclization | 3denopamine arbutamine | 3enantio diastereoselective | 2ligand structure | 2vs cycloisomerization | 2natural products | 2synthesis brefeldin | 24-aryloxybutenolides chiral | 2structure zinc-catalyzed | 2synthetic tool | 2pd catalyzed | 2bis-homopropargylic alcohols | 2aldehyde equivalents | 2ru catalyzed | 2molybdenum-catalyzed asymmetric | 2cyclization vs | 2effect ligand | 2synthesis trisubstituted | 2powerful synthetic | 2alkenes ru-catalyzed | 2cycloisomerization bis-homopropargylic | 2coupling partners | 2equivalents efficient
- 7asymmetric allylic alkylation | 3efficient enantioselective synthesis | 3palladium-catalyzed asymmetric allylic | 3enantio diastereoselective synthesis | 3assignment absolute relative | 3absolute relative configuration | 2structure zinc-catalyzed henry | 2enantioselective synthesis brefeldin | 2zinc-catalyzed henry reaction | 24-aryloxybutenolides chiral aldehyde | 2syntheses denopamine arbutamine | 2effect ligand structure | 2divergence oxidative cyclization | 2chiral aldehyde equivalents | 2cycloisomerization bis-homopropargylic alcohols | 2asymmetric syntheses denopamine | 2trisubstituted alkenes ru-catalyzed | 2alkenes ru-catalyzed addition | 2cyclization vs cycloisomerization | 2ru catalyzed divergence | 2powerful synthetic tool | 2vs cycloisomerization bis-homopropargylic | 2catalyzed asymmetric allylic | 2catalyzed divergence oxidative | 2ligand structure zinc-catalyzed | 2aldehyde equivalents efficient | 2oxidative cyclization vs | 2equivalents efficient enantioselective | 2synthesis trisubstituted alkenes | 2intramolecular palladium-catalyzed allylic | 2reactions atom economy | 2pf catalyzed enyne
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