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Chembiochem : a European Journal of Chemical Biology|April 17, 2012
Use of a multicomponent reaction for chemoselective derivatization of multiple classes of metabolitesKyle A Totaro, Babajide O Okandeji, Jason K Sello
Organic Letters|March 8, 2016
Macrocyclization of Unprotected Peptide IsocyanatesAlexander A Vinogradov, Zi-Ning Choo, Kyle A Totaro, et al.
Bioorganic & Medicinal Chemistry|August 23, 2015
Substrate-guided optimization of the syringolins yields potent proteasome inhibitors with activity against leukemia cell linesKyle A Totaro, Dominik Barthelme, Peter T Simpson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2018
Amide-forming chemical ligation via <i>O</i>-acyl hydroxamic acidsDaniel L Dunkelmann, Yuki Hirata, Kyle A Totaro, et al.
ACS Infectious Diseases|February 11, 2017
Rational Design of Selective and Bioactive Inhibitors of the Mycobacterium tuberculosis ProteasomeKyle A Totaro, Dominik Barthelme, Peter T Simpson, et al.
Bioconjugate Chemistry|March 15, 2016
Systematic Investigation of EDC/sNHS-Mediated Bioconjugation Reactions for Carboxylated Peptide SubstratesKyle A Totaro, Xiaoli Liao, Keshab Bhattacharya, et al.
Nature Communications|July 21, 2021
Fully automated fast-flow synthesis of antisense phosphorodiamidate morpholino oligomersChengxi Li, Alex J Callahan, Mark D Simon, et al.
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