Ehrlic Lo

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Biotechnology Based Process for Production of a Disulfide-Bridged Peptide.

Steven H. Chan, Olav K. Lyngberg, M. Witmer, 2016, Bioconjugate chemistry.

Development of a Practical Synthesis of a p38 Kinase Inhibitor via a Safe and Robust Amination

S. Tummala, Paul C. Lobben, S. Leung, 2012 .

Development of an Efficient Synthesis of Two CRF Antagonists for the Treatment of Neurological Disorders

David K. Leahy, B. Su, Jason Zhu, 2010 .

Development of a scaleable process for the synthesis of a next-generation statin

R. Livingston, S. Tummala, S. Ramakrishnan, 2010 .

A stereoselective synthesis of (S)-2-(((3-fluoro-4-methylphenoxy)carbonyl)(1-(4-((5-methyl-2-phenyloxazol-4-yl)methoxy)phenyl)ethyl)amino)acetic acid, a highly potent PPAR α/γ dual agonist

J. Shabaker, Junying Fan, Keming Zhu, 2015 .

Preparation of β-hydroxy-α-amino Acid Using Recombinant d-Threonine Aldolase

C. Hang, Zhiwei Guo, S. Goldberg, 2015 .

Development of a Two-Step, Enantioselective Synthesis of an Amino Alcohol Drug Candidate

Chenchi Wang, C. Hang, Zhiwei Guo, 2015 .

Revisiting the Cleavage of Evans Oxazolidinones with LiOH/H2O2

Jason M. Stevens, G. Beutner, Andrew W. Glace, 2019, Organic Process Research & Development.

Biotechnology Based Process for Production of a Disulfide-Bridged Peptide.

M. Witmer, R. Hanson, J. Bryson, 2016, Bioconjugate chemistry.