Mrinmoy Saha, Ph.D.

2014 Department of Chemistry Oregon State University, Corvallis, OR 
Organic Synthesis
"Mrinmoy Saha"
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Nikolayevskiy H, Robello M, Scerba MT, et al. (2019) The structure-activity profile of mercaptobenzamides' anti-HIV activity suggests that thermodynamics of metabolism is more important than binding affinity to the target. European Journal of Medicinal Chemistry. 178: 818-837
Zheng H, Saha M, Appella DH. (2018) Synthesis of Fmoc-Protected ( S, S)- trans-Cyclopentane Diamine Monomers Enables the Preparation and Study of Conformationally Restricted Peptide Nucleic Acids. Organic Letters
Tagad HD, Debnath S, Clausse V, et al. (2018) Chemical features important for activity in a class of inhibitors targeting the Wip1 flap subdomain. Chemmedchem
Saha M, Scerba MT, Shank NI, et al. (2017) Probing Mercaptobenzamides as HIV Inactivators via Nucleocapsid Protein 7. Chemmedchem
Hartman TL, Yang L, Helfrick AN, et al. (2016) Preclinical evaluation of a mercaptobenzamide and its prodrug for NCp7-Targeted inhibition of human immunodeficiency virus. Antiviral Research
Saha M, Li X, Collett ND, et al. (2016) Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity. The Journal of Organic Chemistry
Veerasamy N, Carlson EC, Collett ND, et al. (2013) Enantioselective approach to quinolizidines: total synthesis of cermizine D and formal syntheses of senepodine G and cermizine C. The Journal of Organic Chemistry. 78: 4779-800
Saha M, Carter RG. (2013) Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine. Organic Letters. 15: 736-9
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