Benjamin S. Lane, Ph.D.
Affiliations: | 2003 | Texas A & M University, College Station, TX, United States |
Area:
medicinal chemistry, combinatorial chemistry, organic syntheses, asymmetric catalysis, and fluorescent dyesGoogle:
"Benjamin Lane"Parents
Sign in to add mentorKevin Burgess | grad student | 2003 | Texas A & M | |
(Metal-catalyzed epoxidation reactions with hydrogen peroxide.) |
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Publications
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Austad BC, Hague AB, White P, et al. (2016) Development of a Multi Kilogram-Scale, Tandem Cyclopropanation Ring-Expansion Reaction en Route to Hedgehog Antagonist IPI-926 Organic Process Research and Development. 20: 786-798 |
Lane BS, Brown aMA, Sames D. (2007) Direct Palladium-Catalyzed C-2 and C-3 Arylation of Indoles: A Mechanistic Rationale for Regioselectivity [J. Am. Chem. Soc. 2005, 127, 8050−8057]. Journal of the American Chemical Society. 129: 241-241 |
Touré BB, Lane BS, Sames D. (2006) Catalytic C-H arylation of SEM-protected azoles with palladium complexes of NHCs and phosphines. Organic Letters. 8: 1979-82 |
Lane BS, Brown MA, Sames D. (2005) Direct palladium-catalyzed C-2 and C-3 arylation of indoles: a mechanistic rationale for regioselectivity. Journal of the American Chemical Society. 127: 8050-7 |
Wang X, Lane BS, Sames D. (2005) Direct C-arylation of free (NH)-indoles and pyrroles catalyzed by Ar-Rh(III) complexes assembled in situ. Journal of the American Chemical Society. 127: 4996-7 |
Lane BS, Sames D. (2004) Direct C-H bond arylation: selective palladium-catalyzed C2-arylation of N-substituted indoles. Organic Letters. 6: 2897-900 |
Lane BS, Burgess K. (2003) Metal-catalyzed epoxidations of alkenes with hydrogen peroxide. Chemical Reviews. 103: 2457-73 |
Gao MZ, Gao J, Lane BS, et al. (2003) An amino acid co-catalyzed asymmetric aldol reaction Chemistry Letters. 32: 524-525 |
Lane BS, Vogt M, DeRose VJ, et al. (2002) Manganese-catalyzed epoxidations of alkenes in bicarbonate solutions. Journal of the American Chemical Society. 124: 11946-54 |
Lane BS, Burgess K. (2001) A cheap, catalytic, scalable, and environmentally benign method for alkene epoxidations. Journal of the American Chemical Society. 123: 2933-4 |