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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", "enantio diastereoselective synthesis" and "allylic alkylation aaa". 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.

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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]

  • Barry M Trost - Coauthors & Social Network in 2002Barry M Trost - Unique Vocabulary, Keywords and Interests in 2002

Historical Performance Charts [graphical overview of Barry M Trost publication and funding history for the range of years]

  • Barry M Trost - Publications and Funding History in 2002

Emails (3) [email addresses extracted from Barry M Trost affiliations]

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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 | 35Ligands | 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 | 7alkynes | 7ruthenium-catalyzed | 7coupling | 7using | 7efficient | 7enantioselective | 7alkenes | 6cycloisomerization | 6synthetic | 6olefin | 6ligands | 6stereochemistry | 5mechanism | 5enantio | 5different | 5dmf | 5latter | 5baylis-hillman | 5diastereoselective | 5palladium-catalyzed | 5pd-catalyzed | 5absolute
  • 15allylic alkylation | 11asymmetric allylic | 8total synthesis | 4enantio diastereoselective | 4baylis-hillman adducts | 4reaction text | 4enantioselective synthesis | 4trisubstituted alkenes | 3reaction synthesis | 3ruthenium-catalyzed three-component | 3palladium-catalyzed asymmetric | 3alkylation aaa | 3absolute relative | 3catalyzed asymmetric | 3oxidative cyclization | 3synthesis brefeldin | 3aaa reaction | 3pd catalyzed | 3synthesis c-2-epi-hygromycin | 3vinyl halides | 3efficient enantioselective | 3relative configuration | 3formation vinyl | 3assignment absolute | 3diastereoselective synthesis | 3synthesis furaquinocin | 3denopamine arbutamine | 3three-component coupling | 3henry reaction | 2dynamic kinetic | 2application aaa | 2configuration evaluation
  • 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 | 2pd catalyzed asymmetric | 2adducts concise total | 2ru catalyzed divergence | 2concise total synthesis | 2total synthesis c-2-epi-hygromycin | 2inventing reactions atom | 2aldehyde equivalents efficient | 2dykat baylis-hillman adducts | 2cycloisomerization bis-homopropargylic alcohols | 2total synthesis furaquinocin | 2reaction synthesis furanoside | 2ligand structure zinc-catalyzed | 2halides via ruthenium-catalyzed | 2formation vinyl halides | 2aaa reaction synthesis | 2cyclization vs cycloisomerization | 2alkylation enantio diastereoselective | 2synthesis furanoside c-2-epi-hygromycin | 2furanoside c-2-epi-hygromycin total | 2zinc-catalyzed henry reaction | 2dynamic kinetic asymmetric | 24-aryloxybutenolides chiral aldehyde | 2vs cycloisomerization bis-homopropargylic

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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 YearAward 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 YearAward Amount, USD
    5R37GM013598-271992$283,462
    4R37GM013598-281993$420,641
    5R37GM013598-291994$416,614
    5R37GM013598-301995$420,845
    5R37GM013598-311996$435,548
    5R37GM013598-321997$452,970
    2R01GM013598-331998$440,616
    5R01GM013598-341999$423,083
    5R01GM013598-352000$432,932
    5R01GM013598-362001$443,079
    2R01GM013598-372002$521,769
    5R01GM013598-382003$519,106
    5R01GM013598-392004$524,128
    5R01GM013598-402005$537,542
    2R01GM013598-41A12006$569,086
    Total up to 2002$6,841,421
  • NOVEL APPROACHES TO ANTITUMOR AND ANTIVIRAL AGENTS (TROST, BARRY M, STANFORD UNIVERSITY - 1992)
    Grant #Award YearAward Amount, USD
    5R01GM033049-161992$263,430
    2R01GM033049-181993$285,191
    5R01GM033049-171993$282,424
    5R01GM033049-191994$135,972
    5R01GM033049-201995$307,517
    5R01GM033049-211996$305,466
    2R01GM033049-221997$280,340
    5R01GM033049-231998$273,612
    5R01GM033049-241999$280,905
    5R01GM033049-252000$288,504
    2R01GM033049-262001$380,569
    5R01GM033049-282003$375,037
    5R01GM033049-292004$386,074
    2R01GM033049-30A12005$366,006
    5R01GM033049-312006$361,447
    Total up to 2002$4,572,494

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.