B. Sullivan

发表

Library construction and evaluation for site saturation mutagenesis.

J. Stewart, Adam Z. Walton, B. Sullivan, 2013, Enzyme and microbial technology.

Biocatalytic Reductions of Baylis-Hillman Adducts

J. Stewart, Adam Z. Walton, Y. Pompeu, 2011 .

Cytotoxic properties of DAB486EGF and DAB389EGF, epidermal growth factor (EGF) receptor-targeted fusion toxins.

J. Shaw, B. Sullivan, J. Nichols, 1991, The Journal of biological chemistry.

Symmetry-based design for the chemoenzymatic synthesis of oseltamivir (Tamiflu) from ethyl benzoate.

T. Hudlický, B. Sullivan, Ignacio Carrera, 2009, Angewandte Chemie.

Investigation of steric and functionality limits in the enzymatic dihydroxylation of benzoate esters. Versatile intermediates for the synthesis of pseudo-sugars, amino cyclitols, and bicyclic ring systems.

Tomas Hudlicky, T. Hudlický, Hannes G. Leisch, 2009, Organic & biomolecular chemistry.

Several generations of chemoenzymatic synthesis of oseltamivir (Tamiflu): evolution of strategy, quest for a process-quality synthesis, and evaluation of efficiency metrics.

John Andraos, Tomas Hudlicky, T. Hudlický, 2011, The Journal of organic chemistry.

Formal total synthesis of (–)- and (+)-balanol: two complementary enantiodivergent routes from vinyloxiranes and vinylaziridines

T. Hudlický, B. Sullivan, Jacqueline Gilmet, 2009 .

Chemoenzymatic formal synthesis of (−)-balanol. Provision of optical data for an often-reported intermediate

T. Hudlický, B. Sullivan, 2008 .

Structural and Catalytic Characterization of Pichia stipitis OYE 2.6, a Useful Biocatalyst for Asymmetric Alkene Reductions

J. Stewart, Adam Z. Walton, Y. Pompeu, 2012 .

Residues Controlling Facial Selectivity in an Alkene Reductase and Semirational Alterations to Create Stereocomplementary Variants

J. Stewart, Adam Z. Walton, B. Sullivan, 2014, ACS catalysis.

X-ray Crystallography Reveals How Subtle Changes Control the Orientation of Substrate Binding in an Alkene Reductase

J. Stewart, Y. Pompeu, B. Sullivan, 2013 .

Pichia stipitis OYE 2.6 variants with improved catalytic efficiencies from site-saturation mutagenesis libraries.

J. Stewart, B. Sullivan, A. Patterson-Orazem, 2014, Bioorganic & medicinal chemistry.

Synthesis of heterobifunctional polyethylene glycols: Polymerization from functional initiators

Kevin N Sill, B. Sullivan, T. Vojkovský, 2016 .

New Options for the Reactivity of the Burgess Reagent with Epoxides in Both Racemic and Chiral Auxiliary Modes – Structural and Mechanistic Revisions, Computational Studies, and Application to Synthesis

T. Hudlický, Hannes G. Leisch, B. Sullivan, 2009 .

Large-scale synthesis of α-amino acid-N-carboxyanhydrides

Kevin N Sill, B. Sullivan, J. E. Semple, 2017 .

Synthesis and facile end‐group quantification of functionalized PEG azides

Kevin N Sill, B. Sullivan, T. Vojkovský, 2016, Journal of polymer science. Part A, Polymer chemistry.

Synthesis and Characterization of Micelle-Forming PEG-Poly(Amino Acid) Copolymers with Iron-Hydroxamate Cross-Linkable Blocks for Encapsulation and Release of Hydrophobic Drugs.

Kevin N Sill, B. Sullivan, J. E. Semple, 2017, Biomacromolecules.

Enoate Reductases for Reduction of Electron Deficient Alkenes

F. Parmeggiani, B. Turchetti, P. Buzzini, 2012 .

Imaging the delivery of drug-loaded, iron-stabilized micelles.

Kevin N Sill, G. Martinez, B. Sullivan, 2017, Nanomedicine : nanotechnology, biology, and medicine.

Stabilized Polymer Micelles for the Development of IT-147, an Epothilone D Drug-Loaded Formulation

Kevin N Sill, B. Sullivan, J. E. Semple, 2016, Journal of drug delivery.

IT-143, A Polymer Micelle Nanoparticle, Widens Therapeutic Window of Daunorubicin

Kevin N Sill, B. Sullivan, J. E. Semple, 2016 .

Enhancing the heat stability and kinetic parameters of the maize endosperm ADP-glucose pyrophosphorylase using iterative saturation mutagenesis.

L. C. Hannah, J. Stewart, B. Sullivan, 2015, Archives of biochemistry and biophysics.

Synthesis and Characterization of Micelle-Forming PEG-Poly(Amino Acid) Copolymers with Iron-Hydroxamate Cross-Linkable Blocks for Encapsulation and Release of Hydrophobic Drugs.

B. Sullivan, A. Carie, Kevin Sill, 2017, Biomacromolecules.