Gregory G. Springsteen

Ni, W. J., Kaur, G., Springsteen, G., Wang, B. H., & Franzen, S. (2004). Regulating the fluorescence intensity of an anthracene boronic acid system: a B-N bond or a hydrolysis mechanism? BIOORGANIC CHEMISTRY, 32(6), 571–581. https://doi.org/10.1016/j.bioorg.2004.06.004

Ni, W. J., Fang, H., Springsteen, G., & Wang, B. H. (2004). The design of boronic acid spectroscopic reporter compounds by taking advantage of the pK(a)-lowering effect of diol binding: Nitrophenol-based color reporters for diols. JOURNAL OF ORGANIC CHEMISTRY, 69(6), 1999–2007. https://doi.org/10.1021/jo0350357

Yang, W. Q., Yan, J., Springsteen, G., Deeter, S., & Wang, B. H. (2003). A novel type of fluorescent boronic acid that shows large fluorescence intensity changes upon binding with a carbohydrate in aqueous solution at physiological pH. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 13(6), 1019–1022. https://doi.org/10.1016/S0960-894X(03)00086-6

Springsteen, G., & Wang, B. H. (2002). A detailed examination of boronic acid-diol complexation. TETRAHEDRON, 58(26), 5291–5300. https://doi.org/10.1016/S0040-4020(02)00489-1

Yang, W. Q., Gao, X. M., Springsteen, G., & Wang, B. H. (2002). Catechol pendant polystyrene for solid-phase synthesis. TETRAHEDRON LETTERS, 43(36), 6339–6342. https://doi.org/10.1016/S0040-4039(02)01370-9

Springsteen, G., & Wang, B. H. (2001). Alizarin Red S. as a general optical reporter for studying the binding of boronic acids with carbohydrates. Chemical Communications (Cambridge, England), (17), 1608–1609.

Latta, R., Springsteen, G., & Wang, B. H. (2001). Development and synthesis of an arylboronic acid-based solid-phase amidation catalyst. Synthesis (Stuttgart), (11), 1611–1613.

Springsteen, G., Ballard, C. E., Gao, S., Wang, W., & Wang, B. H. (2001). The development of photometric sensors for boronic acids. BIOORGANIC CHEMISTRY, 29(5), 259–270. https://doi.org/10.1006/bioo.2001.1217

Wang, W., Springsteen, G., Gao, S. H., & Wang, B. H. (2000). The first fluorescent sensor for boronic and boric acids with sensitivity at sub-micromolar concentrations. Chemical Communications (Cambridge, England), (14), 1283–1284.