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30Barry M Trost
![]() Summary for 2002 [at-glance overview of Barry M Trost work for the selected year as suggested by data mining algorithms]This is an Authoratory overview of author Barry M Trost. According to available data, in 2002 Barry M Trost published at least 30 articles. This work was completed in collaboration with several authors including Yeh, Vince S C and Hughes, David L. Many other authors have collaborated with Barry M Trost as well. At least 3 different grants are awarded to Barry M Trost to support this work. All time total of the grant awards on file exceeds $14,330,403.
Barry M Trost is a key opinion leader in numerous areas including Catalysis, Stereoisomerism, Alkylation, Palladium, Ruthenium. This author's highest rank is 1 when compared to all other authors using the keyword Catalysis. Analysis of the article abstracts and the titles suggests that Barry M Trost professional interests are focused around "asymmetric allylic alkylation", "assignment absolute relative" and "absolute relative configuration". These might also be referred to as "allylic alkylation", "asymmetric allylic" or "total synthesis". Statistical analysis shows that Barry M Trost's writing is likely to contains terms "synthesis", "asymmetric", "reaction", "allylic", "alkylation" and "formation".
The majority of Barry M Trost articles are affiliated with Department of Chemistry, Stanford University, Stanford, California CA 94305-5080, USA. Luckily, several email addresses are on file. Images [images we found on the Internet for Barry M Trost]loading...
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Alternative names (1) [other authors with names similar to Barry M Trost]Year 2002 Charts [Barry M Trost frequent coauthors and the most common unique vocabulary terms for the selected year]Historical Performance Charts [graphical overview of Barry M Trost publication and funding history for the range of years]Emails (3) [email addresses extracted from Barry M Trost affiliations]hidden to prevent spam, click here to reveal Barry M Trost Coauthors (24) [all coauthors with the number of joint publications] Other [context-specific ads]Affiliations (3) [condensed summary of the Barry M Trost affiliations, the leading number and the color conveys importance]- 27Department of Chemistry, Stanford University, Stanford, California CA 94305-5080, USA.
2Department of Chemistry, Stanford University, Stanford, CA California 94305, USA. 1Department of Chemistry, Stanford University, Stanford, California, 94305,USA.
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 Structures | 1Pyridines
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 | 11reactions | 10catalyzed | 8total | 8chiral | 7efficient | 7ruthenium-catalyzed | 7enantioselective | 7alkynes | 7coupling | 7using | 7alkenes | 6vinyl | 6use | 6aaa | 6strategy | 6cycloisomerization | 6synthetic | 6pd | 6conditions | 5callipeltoside | 5palladium-catalyzed | 5pd-catalyzed | 5absolute | 5ruthenium | 5dykat | 5utility
- 15allylic alkylation | 11asymmetric allylic | 8total synthesis | 4reaction text | 4enantioselective synthesis | 4baylis-hillman adducts | 4enantio diastereoselective | 4trisubstituted alkenes | 3palladium-catalyzed asymmetric | 3absolute relative | 3oxidative cyclization | 3efficient enantioselective | 3relative configuration | 3formation vinyl | 3assignment absolute | 3ruthenium-catalyzed three-component | 3alkylation aaa | 3synthesis brefeldin | 3aaa reaction | 3pd catalyzed | 3synthesis c-2-epi-hygromycin | 3vinyl halides | 3diastereoselective synthesis | 3synthesis furaquinocin | 3denopamine arbutamine | 3three-component coupling | 2syntheses denopamine | 2ru-catalyzed addition | 2dynamic kinetic | 2application aaa | 2configuration evaluation | 2cyclization vs
- 10asymmetric allylic alkylation | 3assignment absolute relative | 3absolute relative configuration | 3palladium-catalyzed asymmetric allylic | 3efficient enantioselective synthesis | 3enantio diastereoselective synthesis | 3allylic alkylation aaa | 3ruthenium-catalyzed three-component coupling | 2alkylation indolocarbazole pro-aglycons | 2adducts concise total | 2ru catalyzed divergence | 2concise total synthesis | 2total synthesis c-2-epi-hygromycin | 2alkenes ru-catalyzed addition | 2aldehyde equivalents efficient | 2dykat baylis-hillman adducts | 2trisubstituted alkenes ru-catalyzed | 2cycloisomerization bis-homopropargylic alcohols | 2total synthesis furaquinocin | 2reaction synthesis furanoside | 2halides via ruthenium-catalyzed | 2formation vinyl halides | 2powerful synthetic tool | 2aaa reaction synthesis | 2cyclization vs cycloisomerization | 2allylic alkylation indolocarbazole | 2alkylation enantio diastereoselective | 2synthesis furanoside c-2-epi-hygromycin | 2synthesis trisubstituted alkenes | 2syntheses denopamine arbutamine | 2furanoside c-2-epi-hygromycin total | 2dynamic kinetic asymmetric
Reader's Comments (1) [comments posted by readers of Barry M Trost profile]Reader Comment: [Trost, Barry M] in 2007 [posted by admin on Wed, 01 Aug 2007 01:45:33 GMT] More information about Barry M. Trost can be found on the home page of The Trost Research Group at Stanford University. Funding (3) [selected NIH grants to Barry M Trost and the award amounts for recent years]- NOVEL SYNTHETIC APPROACHES TO ANTITUMOR AGENTS (TROST, BARRY - 1977)
| Grant # | Award Year | Award Amount, USD | | award information is not available | | Total up to 2002 | $NA |
- SYNTHESIS OF MACROLIDES, STEROIDS, CYCLOPENTANOIDS, ETC. (TROST, BARRY M, STANFORD UNIVERSITY - 1992)
| Grant # | Award Year | Award Amount, USD | | 5R37GM013598-27 | 1992 | $283,462 | | 4R37GM013598-28 | 1993 | $420,641 | | 5R37GM013598-29 | 1994 | $416,614 | | 5R37GM013598-30 | 1995 | $420,845 | | 5R37GM013598-31 | 1996 | $435,548 | | 5R37GM013598-32 | 1997 | $452,970 | | 2R01GM013598-33 | 1998 | $440,616 | | 5R01GM013598-34 | 1999 | $423,083 | | 5R01GM013598-35 | 2000 | $432,932 | | 5R01GM013598-36 | 2001 | $443,079 | | 2R01GM013598-37 | 2002 | $521,769 | | 5R01GM013598-38 | 2003 | $519,106 | | 5R01GM013598-39 | 2004 | $524,128 | | 5R01GM013598-40 | 2005 | $537,542 | | Total up to 2002 | $6,272,335 |
- NOVEL APPROACHES TO ANTITUMOR AND ANTIVIRAL AGENTS (TROST, BARRY M, STANFORD UNIVERSITY - 1992)
| Grant # | Award Year | Award Amount, USD | | 5R01GM033049-16 | 1992 | $263,430 | | 2R01GM033049-18 | 1993 | $285,191 | | 5R01GM033049-17 | 1993 | $282,424 | | 5R01GM033049-19 | 1994 | $135,972 | | 5R01GM033049-20 | 1995 | $307,517 | | 5R01GM033049-21 | 1996 | $305,466 | | 2R01GM033049-22 | 1997 | $280,340 | | 5R01GM033049-23 | 1998 | $273,612 | | 5R01GM033049-24 | 1999 | $280,905 | | 5R01GM033049-25 | 2000 | $288,504 | | 2R01GM033049-26 | 2001 | $380,569 | | 5R01GM033049-28 | 2003 | $375,037 | | 5R01GM033049-29 | 2004 | $386,074 | | 2R01GM033049-30A1 | 2005 | $366,006 | | Total up to 2002 | $4,211,047 |
Barry M Trost Articles (30) [selected PubMed articles for the year 2002 with the links to a full text at PubMed]Utilization of molybdenum- and palladium-catayzed dynamic kinetic asymmetric transformations for the preparation of tertiary and quaternary stereogenic centers: a concise synthesis of tipranavir. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 30Trost, Barry M, 1Andersen, Neil G.Enantioselective synthesis of (-)-codeine and (-)-morphine. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 3Tang, Weiping, 30Trost, Barry M.An efficient one-pot enantio- and diastereoselective synthesis of heterocycles. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 30Trost, Barry M, 1Machacek, Michelle R.Polymer-supported C2-symmetric ligands for palladium-catalyzed asymmetric allylic alkylation reactions. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 1Pan, Zhengying, 1Kujat, Christof, 30Trost, Barry M, 1Zambrano, Jorge.An acid-catalyzed macrolactonization protocol. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 30Trost, Barry M, 4Chisholm, John D.Intramolecular palladium-catalyzed allylic alkylation: enantio- and diastereoselective synthesis of [2.2.2] bicycles. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 1Sacchi, Karna L, 30Trost, Barry M, 1Asakawa, Naoyuki, 2Schroeder, Gretchen M.Stereocontrolled synthesis of (+)-boronolide. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 3Yeh, Vince S C, 30Trost, Barry M.Ruthenium-catalyzed alkene-alkyne coupling: synthesis of the proposed structure of amphidinolide A. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 1Jung, Michael, 30Trost, Barry M, 4Chisholm, John D, 1Wrobleski, Stephen T.The unusual role of CO transfer in molybdenum-catalyzed asymmetric alkylations. (2002) >> Department of Chemistry, Stanford University, California 94305-5080, USA. 2Sun, Yongkui, 1Mathre, David J, 9Hughes, David L, 30Trost, Barry M, 7Reamer, Robert A, 1Krska, Shane W.DYKAT of Baylis-Hillman adducts: concise total synthesis of furaquinocin E. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 30Trost, Barry M, 1Tsui, Hon-Chung, 1Thiel, Oliver R.Palladium-catalyzed asymmetric allylic alkylation of alpha-aryl ketones. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 30Trost, Barry M, 2Schroeder, Gretchen M, 1Kristensen, Jesper.Callipeltoside a: total synthesis, assignment of the absolute and relative configuration, and evaluation of synthetic analogues. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 3Dirat, Olivier, 2Gunzner, Janet L, 30Trost, Barry M, 1Rhee, Young H.On inventing reactions for atom economy. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 30Trost, Barry M.An efficient enantioselective synthesis of (-)-galanthamine. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 3Tang, Weiping, 30Trost, Barry M.Effect of ligand structure on the zinc-catalyzed Henry reaction. Asymmetric syntheses of (-)-denopamine and (-)-arbutamine. (2002) >> Department of Chemistry, Stanford University, California 94305-5080, USA. 1Ito, Hisanako, 3Yeh, Vince S C, 30Trost, Barry M, 1Bremeyer, Nadine.4-Aryloxybutenolides as "chiral aldehyde" equivalents: an efficient enantioselective synthesis of (+)-brefeldin a. (2002) >> Department of Chemistry, Stanford University, California 94305-5080, USA. 1Crawley, Matthew L, 30Trost, Barry M.A chemoselective reduction of alkynes to (E)-alkenes. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 2Ball, Zachary T, 30Trost, Barry M, 1Jöge, Thomas.Designed ligands as probes for the catalytic binding mode in Mo-catalyzed asymmetric allylic alkylation. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305, USA. 9Hughes, David L, 2Hachiya, Iwao, 1Emura, Takashi, 30Trost, Barry M, 7Reamer, Robert A, 2Dogra, Kalindi, 14Reider, Paul J, 4Yasuda, Nobuyoshi, 1Krska, Shane, 3Palucki, Michael.Synthesis of novel quaternary amino acids using molybdenum-catalyzed asymmetric allylic alkylation. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 30Trost, Barry M, 2Dogra, Kalindi.Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 7Krische, Michael J, 2Berl, Volker, 30Trost, Barry M, 1Grenzer, Ellen M.Formation of vinyl halides via a ruthenium-catalyzed three-component coupling. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305, USA. 30Trost, Barry M, 2Pinkerton, Anthony B.A synthesis of trisubstituted alkenes by a Ru-catalyzed addition. (2002) >> Department of Chemistry, Stanford University Stanford, CA 94305-5080, USA. 1Shen, Hong C, 30Trost, Barry M, 2Pinkerton, Anthony B.Mechanistic dichotomy in CpRu(CH(3)CN)(3)PF(6) catalyzed enyne cycloisomerizations. (2002) >> Department of Chemistry, Stanford University, Stanford, California, 94305,USA. 1Toste, F Dean, 30Trost, Barry M.An unusual ruthenium-catalyzed cycloisomerization of alkynes and propargyl alcohols. (2002) >> Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. 30Trost, Barry M, 2Rudd, Michael T.A dinuclear Zn catalyst for the asymmetric nitroaldol (Henry) reaction. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 3Yeh, Vince S C, 30Trost, Barry M.A Ru catalyzed divergence: oxidative cyclization vs cycloisomerization of bis-homopropargylic alcohols. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 1Rhee, Young Ho, 30Trost, Barry M.A stereospecific ruthenium-catalyzed allylic alkylation. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 2Ball, Zachary T, 30Trost, Barry M, 1Fraisse, Pierre L.Callipeltoside A: assignment of absolute and relative configuration by total synthesis. (2002) >> Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. 3Dirat, Olivier, 2Gunzner, Janet L, 30Trost, Barry M.Application of the AAA reaction to the synthesis of the furanoside of C-2-epi-hygromycin A: a total synthesis of C-2-epi-hygromycin A. (2002) >> Department of Chemistry, Stanford University, CA 94305-5080, USA. 3Dirat, Olivier, 30Trost, Barry M, 1Dudash, Joseph.Pd asymmetric allylic alkylation (AAA). A powerful synthetic tool. (2002) >> Department of Chemistry, Stanford University, CA 94305-5080, USA. 30Trost, Barry M.
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