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29Barry 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 29 articles. This work was completed in collaboration with several authors including Yeh, Vince S C and Chisholm, John D. 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 $12,949,660.

Barry M Trost is a key opinion leader in numerous areas including Catalysis, Stereoisomerism, Ruthenium, Alkylation, Palladium. 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 "efficient enantioselective synthesis". 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", "allylic", "reaction", "alkylation" and "reactions".

The majority of Barry M Trost articles are affiliated with Department of Chemistry, Stanford University, Stanford, California 94305, 94305-5080, USA and Department of Chemistry, Stanford University, Stanford, 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]

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]

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Barry M Trost Coauthors (18) [all coauthors with the number of joint publications]

3

3Yeh, Vince S C

2

4Chisholm, John D

2

3Tang, Weiping

2

2Ball, Zachary T

2

2Pinkerton, Anthony B

2

2Schroeder, Gretchen M

1

8Hughes, David L

1

7Krische, Michael J

1

6Reamer, Robert A

1

2Rudd, Michael T

1

2Sun, Yongkui

1

1Crawley, Matthew L

1

1Jung, Michael

1

1Krska, Shane W

1

1Mathre, David J

1

1Shen, Hong C

1

1Toste, F Dean

1

1Wrobleski, Stephen T

 

Affiliations (3) [condensed summary of the Barry M Trost affiliations, the leading number and the color conveys importance]

  • 14Department of Chemistry, Stanford University, Stanford, California 94305, 94305-5080, USA.
    14Department of Chemistry, Stanford University, Stanford, CA 94305-5080, 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]

  • 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

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 | 6formation | 6enantioselective | 6ruthenium-catalyzed | 6cycloisomerization | 5palladium-catalyzed | 5mechanism | 5c-2-epi-hygromycin | 5synthetic | 5efficient | 5trisubstituted | 5coupling | 5chiral | 4pd | 4strategy | 4utility | 4absolute | 4structure | 4can | 4syntheses | 4vinyl | 4proposed | 3bond
  • 12allylic alkylation | 8asymmetric allylic | 7total synthesis | 4enantioselective synthesis | 4trisubstituted alkenes | 3palladium-catalyzed asymmetric | 3vinyl halides | 3oxidative cyclization | 3absolute relative | 3relative configuration | 3denopamine arbutamine | 3synthesis c-2-epi-hygromycin | 3efficient enantioselective | 3assignment absolute | 2inventing reactions | 2ruthenium-catalyzed three-component | 2reactions atom | 2c-2-epi-hygromycin total | 2evaluation synthetic | 2regio enantioselective | 2synthesis brefeldin | 24-aryloxybutenolides chiral | 2indolocarbazole pro-aglycons | 2synthesis assignment | 2synthetic tool | 2via ruthenium-catalyzed | 2pd catalyzed | 2formation vinyl | 2aldehyde equivalents | 2reaction synthesis | 2cpru ch | 2alkylation indolocarbazole
  • 7asymmetric allylic alkylation | 3assignment absolute relative | 3efficient enantioselective synthesis | 3absolute relative configuration | 3palladium-catalyzed asymmetric allylic | 2reactions atom economy | 2pf catalyzed enyne | 2application aaa reaction | 2enantioselective synthesis brefeldin | 24-aryloxybutenolides chiral aldehyde | 2syntheses denopamine arbutamine | 2alkylation indolocarbazole pro-aglycons | 2synthesis assignment absolute | 2reaction synthesis furanoside | 2halides via ruthenium-catalyzed | 2evaluation synthetic analogues | 2cpru ch cn | 2furanoside c-2-epi-hygromycin total | 2pd-catalyzed allylic alkylation | 2via ruthenium-catalyzed three-component | 2chiral aldehyde equivalents | 2relative configuration evaluation | 2inventing reactions atom | 2aaa reaction synthesis | 2dichotomy cpru ch | 2asymmetric syntheses denopamine | 2trisubstituted alkenes ru-catalyzed | 2alkenes ru-catalyzed addition | 2cn pf catalyzed | 2total synthesis c-2-epi-hygromycin | 2ruthenium-catalyzed three-component coupling | 2mechanistic dichotomy cpru

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 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
    Total up to 2002$5,210,665
  • 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
    Total up to 2002$3,458,967

Barry M Trost Articles (29) [selected PubMed articles for the year 2002 with the links to a full text at PubMed]

  • Enantioselective synthesis of (-)-codeine and (-)-morphine. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    3Tang, Weiping, 29Trost, Barry M.

  • 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.

    1Andersen, Neil G, 29Trost, Barry M.

  • An efficient one-pot enantio- and diastereoselective synthesis of heterocycles. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    1Machacek, Michelle R, 29Trost, Barry M.

  • Polymer-supported C2-symmetric ligands for palladium-catalyzed asymmetric allylic alkylation reactions. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    1Kujat, Christof, 29Trost, Barry M, 1Zambrano, Jorge, 1Pan, Zhengying.

  • 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.

    29Trost, Barry M, 1Asakawa, Naoyuki, 2Schroeder, Gretchen M, 1Sacchi, Karna L.

  • Stereocontrolled synthesis of (+)-boronolide. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    3Yeh, Vince S C, 29Trost, Barry M.

  • The unusual role of CO transfer in molybdenum-catalyzed asymmetric alkylations. (2002) >>

    Department of Chemistry, Stanford University, California 94305-5080, USA.

    1Mathre, David J, 1Krska, Shane W, 2Sun, Yongkui, 8Hughes, David L, 29Trost, Barry M, 6Reamer, Robert A.

  • An acid-catalyzed macrolactonization protocol. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    4Chisholm, John D, 29Trost, 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.

    4Chisholm, John D, 29Trost, Barry M, 1Jung, Michael, 1Wrobleski, Stephen T.

  • DYKAT of Baylis-Hillman adducts: concise total synthesis of furaquinocin E. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    1Thiel, Oliver R, 29Trost, Barry M, 1Tsui, Hon-Chung.

  • On inventing reactions for atom economy. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    29Trost, Barry M.

  • 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.

    2Gunzner, Janet L, 1Rhee, Young H, 29Trost, Barry M, 3Dirat, Olivier.

  • Palladium-catalyzed asymmetric allylic alkylation of alpha-aryl ketones. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    1Kristensen, Jesper, 29Trost, Barry M, 2Schroeder, Gretchen M.

  • 4-Aryloxybutenolides as "chiral aldehyde" equivalents: an efficient enantioselective synthesis of (+)-brefeldin a. (2002) >>

    Department of Chemistry, Stanford University, California 94305-5080, USA.

    29Trost, Barry M, 1Crawley, Matthew L.

  • 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.

    3Yeh, Vince S C, 1Ito, Hisanako, 29Trost, Barry M, 1Bremeyer, Nadine.

  • An efficient enantioselective synthesis of (-)-galanthamine. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    3Tang, Weiping, 29Trost, Barry M.

  • A chemoselective reduction of alkynes to (E)-alkenes. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    29Trost, Barry M, 1Jöge, Thomas, 2Ball, Zachary T.

  • Formation of vinyl halides via a ruthenium-catalyzed three-component coupling. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305, USA.

    2Pinkerton, Anthony B, 29Trost, Barry M.

  • Synthesis of novel quaternary amino acids using molybdenum-catalyzed asymmetric allylic alkylation. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    1Dogra, Kalindi, 29Trost, Barry M.

  • Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    1Grenzer, Ellen M, 29Trost, Barry M, 2Berl, Volker, 7Krische, Michael J.

  • A synthesis of trisubstituted alkenes by a Ru-catalyzed addition. (2002) >>

    Department of Chemistry, Stanford University Stanford, CA 94305-5080, USA.

    2Pinkerton, Anthony B, 1Shen, Hong C, 29Trost, Barry M.

  • 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, 29Trost, Barry M.

  • An unusual ruthenium-catalyzed cycloisomerization of alkynes and propargyl alcohols. (2002) >>

    Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

    29Trost, 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, 29Trost, 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.

    29Trost, Barry M, 1Rhee, Young Ho.

  • Callipeltoside A: assignment of absolute and relative configuration by total synthesis. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    2Gunzner, Janet L, 29Trost, Barry M, 3Dirat, Olivier.

  • A stereospecific ruthenium-catalyzed allylic alkylation. (2002) >>

    Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA.

    1Fraisse, Pierre L, 29Trost, Barry M, 2Ball, Zachary T.

  • Pd asymmetric allylic alkylation (AAA). A powerful synthetic tool. (2002) >>

    Department of Chemistry, Stanford University, CA 94305-5080, USA.

    29Trost, 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.

    29Trost, Barry M, 3Dirat, Olivier, 1Dudash, Joseph.