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30Barry 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]- 1Alkenes | 1Catalysis | 1Lactones | 1Ruthenium | 1Alkynes | 1Stereoisomerism | 1Alkylation | 2Palladium | 4Isomerism | 6Molybdenum | 8Aldehydes | 11Macrolides | 18Organometallic Compounds | 34Ligands | 43Molecular Structure | 173Oxidation-Reduction | 237Anti-Bacterial Agents
Keywords (32) [keywords assigned to Barry M Trost articles by PubMed, the leading number and the color conveys importance]- 20Catalysis | 14Stereoisomerism | 9Alkylation | 8Palladium | 8Ruthenium | 7Alkynes | 6Alkenes | 5Molecular Structure | 4Organometallic Compounds | 4Lactones | 4Ligands | 3Aldehydes | 3Anti-Bacterial Agents | 3Isomerism | 3Macrolides | 3Molybdenum | 3Oxidation-Reduction | 2Propanols | 2Heterocyclic Compounds | 2Allyl Compounds | 2Hydrocarbons, Cyclic | 2Zinc | 2Kinetics | 1Optical Rotation | 1Cholinesterase Inhibitors | 1Pyrones | 1Morphine | 1Phenols | 1Hygromycin B | 1Carbazoles | 1Plant Components | 1Pyridines
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]- 37synthesis | 23asymmetric | 20reaction | 16allylic | 15alkylation | 13formation | 10catalyzed | 8chiral | 8total | 7alkynes | 7enantioselective | 7coupling | 7ruthenium-catalyzed | 7using | 7efficient | 7alkenes | 6aaa | 6strategy | 6vinyl | 6use | 6synthetic | 6olefin | 6conditions | 5dmf | 5absolute | 5dykat | 5utility | 5excellent | 5baylis-hillman | 5ruthenium | 5structure | 5configuration
- 15allylic alkylation | 11asymmetric allylic | 8total synthesis | 4baylis-hillman adducts | 4enantioselective synthesis | 4enantio diastereoselective | 4reaction text | 4trisubstituted alkenes | 3henry reaction | 3ruthenium-catalyzed three-component | 3palladium-catalyzed asymmetric | 3alkylation aaa | 3absolute relative | 3catalyzed asymmetric | 3synthesis brefeldin | 3aaa reaction | 3vinyl halides | 3efficient enantioselective | 3relative configuration | 3formation vinyl | 3assignment absolute | 3diastereoselective synthesis | 3synthesis furaquinocin | 3denopamine arbutamine | 3three-component coupling | 2syntheses denopamine | 2vinyl bromides | 2ch cn | 2zinc-catalyzed henry | 2molybdenum-catalyzed asymmetric | 2adducts concise | 2ligand structure
- 10asymmetric allylic alkylation | 3enantio diastereoselective synthesis | 3allylic alkylation aaa | 3assignment absolute relative | 3absolute relative configuration | 3ruthenium-catalyzed three-component coupling | 3catalyzed asymmetric allylic | 3palladium-catalyzed asymmetric allylic | 3efficient enantioselective synthesis | 2adducts concise total | 2cn pf catalyzed | 2pf catalyzed enyne | 2ch cn pf | 2concise total synthesis | 2dykat baylis-hillman adducts | 2total synthesis furaquinocin | 2ligand structure zinc-catalyzed | 2halides via ruthenium-catalyzed | 2formation vinyl halides | 2powerful synthetic tool | 2dichotomy cpru ch | 2alkylation enantio diastereoselective | 2syntheses denopamine arbutamine | 2zinc-catalyzed henry reaction | 2palladium-catalyzed allylic alkylation | 2effect ligand structure | 2asymmetric syntheses denopamine | 2diastereoselective synthesis bicycles | 2baylis-hillman adducts concise | 2cpru ch cn | 2allylic alkylation enantio | 2catalyzed enyne cycloisomerizations
Science Trivia (2) [Interactive math & science trivia questions]
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