Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033049-17
Application #
3282391
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1987-04-01
Project End
1993-09-04
Budget Start
1993-04-01
Budget End
1993-09-04
Support Year
17
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Arts and Sciences
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Trost, Barry M; Huang, Zhongxing; Murhade, Ganesh M (2018) Catalytic palladium-oxyallyl cycloaddition. Science 362:564-568
Trost, Barry M; Ryan, Michael C (2017) Indenylmetal Catalysis in Organic Synthesis. Angew Chem Int Ed Engl 56:2862-2879
Trost, Barry M; Chan, Walter H; Malhotra, Sushant (2017) Development of the Regiodivergent Asymmetric Prenylation of 3-Substituted Oxindoles. Chemistry 23:4405-4414
Trost, Barry M; Li, Xiaoxun (2017) Pd-catalyzed asymmetric allylic alkylations via C-H activation of N-allyl imines with glycinates. Chem Sci 8:6815-6821
Trost, Barry M; Tracy, Jacob S (2017) Carbon-Nitrogen Bond Formation via the Vanadium Oxo Catalyzed Sigmatropic Functionalization of Allenols. Org Lett 19:2630-2633
Trost, Barry M; Cregg, James J; Quach, Nicolas (2017) Isomerization of N-Allyl Amides To Form Geometrically Defined Di-, Tri-, and Tetrasubstituted Enamides. J Am Chem Soc :
Trost, Barry M; Kalnmals, Christopher A (2017) Stereoselective Synthesis of Exocyclic Tetrasubstituted Vinyl Halides via Ru-Catalyzed Halotropic Cycloisomerization of 1,6-Haloenynes. Org Lett 19:2346-2349
Trost, Barry M; Saget, Tanguy; Hung, Chao-I Joey (2017) Efficient Access to Chiral Trisubstituted Aziridines via Catalytic Enantioselective Aza-Darzens Reactions. Angew Chem Int Ed Engl 56:2440-2444
Trost, Barry M; Sharif, Ehesan U; Cregg, James J (2017) Ru-catalyzed sequence for the synthesis of cyclic amido-ethers. Chem Sci 8:770-774
Trost, Barry M; Gnanamani, Elumalai; Hung, Chao-I Joey (2017) Controlling Regioselectivity in the Enantioselective N-Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc-ProPhenol. Angew Chem Int Ed Engl 56:10451-10456

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