J. Spink

Antibody drug conjugates of cleavable amino-benzoyl-maytansinoids.

N. Papadopoulos, G. Thurston, Jing Shan, 2020, Bioorganic & medicinal chemistry.

Antibody drug conjugates of cleavable amino-alkyl and aryl maytansinoids.

Jason T Giurleo, N. Papadopoulos, G. Thurston, 2018, Bioorganic & medicinal chemistry.

Regio- and diastereoselective ring-opening of (S)-(−)-2-(trifluoromethyl)oxirane with chiral 2,5-disubstituted tetrahydroquinolines in hexafluoro-2-propanol

R. Russell, K. Sorgi, W. Murray, 2010 .

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

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

Synthesis of Mavatrep: A Potent Antagonist of Transient Receptor Potential Vanilloid-1

R. Russell, A. Abdel-Magid, C. Teleha, 2015 .

Process Development for Scale-Up of a Novel 3,5-Substituted Thiazolidine-2,4-dione Compound as a Potent Inhibitor for Estrogen-Related Receptor 1

Hui-Sheng Huang, R. Patch, M. Player, 2014 .