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John Limanto

Affiliations: 
1997 Massachusetts Institute of Technology, Cambridge, MA, United States 
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"John Limanto"
Bio:

http://hdl.handle.net/1721.1/43577

Mean distance: 7.12
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Parents

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Stephen L. Buchwald grad student 1997 MIT
 (M.Sc. thesis Some synthetic applications of 3,4-disubstituted indoles generated via zirconocene-stabilized benzyne complexes)
Marc L. Snapper grad student 2001 Boston College
 (Scope and limitations of intramolecular cycloadditions of cyclobutadiene and application toward the total synthesis of (+)- and (-)-asteriscanolide.)

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Publications

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Pirnot MT, Mao E, Lam YH, et al. (2022) A Diastereoselective Method for the Construction of -2'-Deoxy-2'-fluoronucleosides. Organic Letters
Klapars A, Chung JYL, Limanto J, et al. (2021) Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036
Klapars A, Chung JYL, Limanto J, et al. (2021) Efficient synthesis of antiviral agent uprifosbuvir enabled by new synthetic methods. Chemical Science. 12: 9031-9036
Haidar Ahmad IA, Chen W, Halsey HM, et al. (2019) Multi-column ultra-high performance liquid chromatography screening with chaotropic agents and computer-assisted separation modeling enables process development of new drug substances. The Analyst
Phillips EM, Reibarkh M, Limanto J, et al. (2019) Improved Process for a Copper-Catalyzed C–N Coupling in the Synthesis of Verubecestat Organic Process Research & Development. 23: 1674-1678
Zhong YL, Cleator E, Liu Z, et al. (2018) Highly Diastereoselective Synthesis of A HCV NS5B Nucleoside Polymerase Inhibitor. The Journal of Organic Chemistry
Pirrone GF, Mathew RM, Makarov AA, et al. (2018) Supercritical fluid chromatography-photodiode array detection-electrospray ionization mass spectrometry as a framework for impurity fate mapping in the development and manufacture of drug substances. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 1080: 42-49
DiRocco DA, Ji Y, Sherer EC, et al. (2017) A multifunctional catalyst that stereoselectively assembles prodrugs. Science (New York, N.Y.). 356: 426-430
Hyde AM, Liu Z, Kosjek B, et al. (2016) Synthesis of the GPR40 Partial Agonist MK-8666 through a Kinetically Controlled Dynamic Enzymatic Ketone Reduction. Organic Letters
Limanto J, Yoshikawa N, Reamer RA, et al. (2015) Promotion of a Ti-Mediated Mannich Reaction by a Proton Source. The Journal of Organic Chemistry
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