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Doctoral and Postdoctoral Work

10. Liang, L.; et al.

Liang, L.; Zhang, J.; Zhu, L.; Duarandin, A.; Young Jr., V. G.; Geacintov, N.; Canary, J. W. Structures, Metal Ion Affinities, and Fluorescence Properties of Soluble Derivatives of Tris((6-phenyl-2-pyridyl)methyl)amine. Inorg. Chem. 2009, 48, 11196–11208.

9. Zhu, L.; et al.

Zhu, L.; Shabbir, S. H.; Anslyn, E. V. Two Methods for the Determination of Enantiomeric Excess (ee) and Concentration of a Chiral Sample with a Single Spectroscopic Measurement. Chem. Eur. J. 2007, 13, 99-104.

8. Zhu, L.; et al.

Zhu, L.; Shabbir, S. H.; Gray, M.; Lynch, V. M.; Sorey, S.; Anslyn, E. V. A Structural Investigation of the N-B Interaction in an o-(N,N-Dialkylaminomethyl)arylboronate System. J. Am. Chem. Soc. 2006, 128, 1222-1232.

7. Zhu, L.; Anslyn, E. V.

Zhu, L.; Anslyn, E. V. Signal Amplification via Allosteric Catalysis. Angew. Chem. Int. Ed. 2006, 45, 1190-1196.

6. Zhu, L.; et al.

Zhu, L.; Zhong, Z.; Anslyn, E. V. Guidelines in Implementing Enantioselective Indicator-Displacement Assays for alpha-Hydroxycarboxylates and Diols. J. Am. Chem. Soc. 2005, 127, 4260-4269.

5. Zhu, L.; et al.

Zhu, L.; Lynch, V. M.; Anslyn, E. V. FRET Induced by an “Allosteric” Cycloaddition Reaction Regulated with Exogenous Inhibitor and Effectors. Tetrahedron 2004, 60, 7267-7275.

4. Zhu, L.; Anslyn, E. V.

Zhu, L.; Anslyn, E. V. Facile Quantification of Enantiomeric Excess and Concentration with Indicator-Displacement Assays: An Example in the Analyses of alpha-Hydroxyacids. J. Am. Chem. Soc. 2004, 126, 3676-3677.

3. Zhu, L.; et al.

Zhu, L.; dos Santos, O.; Koo, C. W.; Rybstein, M.; Pape, L.; Canary, J. W. Geometry-Dependent Phosphodiester Hydrolysis Catalyzed by Binuclear Copper Complexes. Inorg. Chem. 2003, 42, 7912-7920.

2. Zhu, L.; et al.

Zhu, L.; Lukeman, P. S.; Canary, J. W.; Seeman, N. C. Nylon-DNA: Single-Stranded DNA with a Covalently Stitched Nylon Lining. J. Am. Chem. Soc. 2003, 125, 10178-10179.

1. Zhu, L.; et al.

Zhu, L.; dos Santos, O.; Seeman, N. C.; Canary, J. W. Reaction of N3-Benzoyl-3’, 5’-O-(di-tert-butylsilanediyl)uridine with Hindered Electrophiles: Intermolecular N3 to 2’-O Protecting Group Transfer. Nucl., Nucl. & Nucl. Acids 2002, 21, 723-735.