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1. chemistry.stanford.edu › people › barry-trostBarry Trost | Chemistry - Stanford University

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   Targets include β-lactam antibiotics, ionophores, steroids and related compounds (e.g., Vitamin D metabolites), alkaloids, nucleosides, carbohydrates, and macrolide, terpenoid, and tetracyclic antitumor and antibiotic agents. Born in Philadelphia, Pennsylvania, Barry Trost began his university training at the University of Pennsylvania (BA ...

2. en.wikipedia.org › wiki › Barry_TrostBarry Trost - Wikipedia

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   Barry M. Trost (born June 13, 1941, in Philadelphia) is an American chemist who is the Job and Gertrud Tamaki Professor Emeritus in the School of Humanities and Sciences at Stanford University. The Tsuji-Trost reaction and the Trost ligand are named after him.

3. web.stanford.edu › group › bmtrostTrost Group Home - Stanford University

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   Mar 30, 2017 · Trost Group Home. _____. ------. Principal Research Interests. Our research program revolves around the theme of synthesis. There are two major activities - 1) developing the tools, i.e., the reactions and reagents, and 2) creating the proper network of reactions to make complex targets readily available from simple starting materials.

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5. profiles.stanford.edu › barry-trostBarry Trost's Profile | Stanford Profiles

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   Barry Trost is a renowned organic chemist who developed many innovative reactions and catalysts for synthesis. He received numerous awards and honors, including the Linus Pauling Medal, the Tetrahedron Prize, and the Ryoji Noyori Prize.

6. web.stanford.edu › group › bmtrostProfessor Trost CV - Stanford University

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   B.M. Trost and H. Ito US Patent 6,610,889 August 26, 2003 "Catalytic Compositions and Methods for Asymmetric Aldol Reactions" B.M. Trost and H. Ito US Patent 6, 919,456 B2 July 19, 2005: This website is designed and maintained by the Trost Group. Please direct all questions or comments to schultz2 at stanford dot edu. Updated on August 15, 2013

7. People also ask

   Who is Barry Trost?

   • Born in Philadelphia, Pennsylvania, Barry Trost began his university training at the University of Pennsylvania (BA, 1962) and completed his Ph.D. in Chemistry at the Massachusetts Institute of Technology (1965).

   Barry Trost | Chemistry - Stanford University

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   Who is Professor Trost?

   • In recognition of his innovations and scholarship in the field of organic synthesis, Professor Trost has received the ACS Award in Pure Chemistry, ACS Award for Creative Work in Synthetic Organic Chemistry, Arthur C. Cope Scholar Award, and the Presidential Green Chemistry Challenge Award, among many others.

   Barry Trost | Chemistry - Stanford University

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   When did John Trost become a professor of Chemistry?

   • Trost moved to the University of Wisconsin–Madison to begin his independent career, and was promoted to professor of chemistry in 1969, and the Vilas Research Professor in 1982. In 1987, he moved to Stanford University as professor of chemistry, and was appointed the Job and Gertrud Tamaki Professor of Humanities and Sciences in 1990.

   Barry Trost - Wikipedia

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   Where did John Trost go to school?

   • Trost was born in Philadelphia, Pennsylvania on June 13, 1941. He studied at the University of Pennsylvania and obtained his B.A. in 1962. He then attended the Massachusetts Institute of Technology for graduate school, where he worked with Herbert O. House on enolate anions, the Mannich reaction, and the Robinson annulation.

   Barry Trost - Wikipedia

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8. scholar.google.com › citations‪Barry Trost‬ - ‪Google Scholar‬

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   2010. Asymmetric syntheses of oxindole and indole spirocyclic alkaloid natural products. BM Trost, MK Brennan. Synthesis 2009 (18), 3003-3025. , 2009. 800. 2009. On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols. BM Trost, JL Belletire, S Godleski, PG McDougal, JM Balkovec, ...

9. web.stanford.edu › group › bmtrostPublications 1994-Present - Stanford University

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   820. Trost, Barry M.; Xu, Jiayi "The O-Acylation of Ketone Enolates by Allyl 1H-Imidazole-1-carboxylate Mediated with Boron Trifluoride Etherate-A Convenient Procedure for the Synthesis of Substituted Allyl Enol Carbonates." Journal of Organic Chemistry (2007), 72, 9372-9375. 819.