Brandon D. Calitree, Ph.D.
Affiliations: | 2012 | Chemistry | State University of New York, Buffalo, Buffalo, NY, United States |
Google:
"Brandon Calitree"Mean distance: 9.1 | S | N | B | C | P |
Parents
Sign in to add mentor| Michael R. Detty | grad student | 2012 | SUNY Buffalo | |
| (Computational Analysis and Synthetic Strategies towards Novel Heavy-Chalcogenorhodamine Analogues for use in Dye-Sensitized Solar Cells, Dye-Sensitized Photocatalysts and the Inhibition of P-Glycoprotein.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Kryman MW, Schamerhorn GA, Hill JE, et al. (2014) Synthesis and Properties of Heavy Chalcogen Analogues of the Texas Reds and Related Rhodamines. Organometallics. 33: 2628-2640 |
| Orchard A, Schamerhorn GA, Calitree BD, et al. (2012) Thiorhodamines containing amide and thioamide functionality as inhibitors of the ATP-binding cassette drug transporter P-glycoprotein (ABCB1). Bioorganic & Medicinal Chemistry. 20: 4290-302 |
| McCormick TM, Calitree BD, Orchard A, et al. (2010) Reductive side of water splitting in artificial photosynthesis: new homogeneous photosystems of great activity and mechanistic insight. Journal of the American Chemical Society. 132: 15480-3 |
| Calitree BD, Detty MR. (2010) Novel rhodamine dyes via suzuki coupling of xanthone triflates with arylboroxins Synlett. 89-92 |
| Sathyamoorthy B, Axelrod A, Farwell V, et al. (2010) Novel 21,23-ditelluraporphyrins and the first 26,28-ditellurasapphyrin and 30,33-ditellurarubyrin Organometallics. 29: 3431-3441 |
| Holt JJ, Calitree BD, Vincek J, et al. (2007) A microwave-assisted synthesis of julolidine-9-carboxamide derivatives and their conversion to chalcogenoxanthones via directed metalation. The Journal of Organic Chemistry. 72: 2690-3 |
| Calitree B, Donnelly DJ, Holt JJ, et al. (2007) Tellurium analogues of rosamine and rhodamine dyes: Synthesis, structure, 125Te NMR, and heteroatom contributions to excitation energies Organometallics. 26: 6248-6257 |