Arvind Jaganathan, Ph.D.
Affiliations: | 2014 | Chemistry | Michigan State University, East Lansing, MI |
Area:
Synthetic and Bioorganic ChemistryGoogle:
"Arvind Jaganathan"Mean distance: 8.71 | S | N | B | C | P |
Parents
Sign in to add mentorBabak Borhan | grad student | 2014 | Michigan State | |
(Development of catalytic, enantioselective halofunctionalization reactions of olefins and the investigation of cyclic orthoesters as synthetic building blocks for chiral molecules.) |
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Publications
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Luderer SE, Masoudi B, Sarkar A, et al. (2023) Structure-Enantioselectivity Relationship (SER) Study of Cinchona Alkaloid Chlorocyclization Catalysts. The Journal of Organic Chemistry |
Salehi Marzijarani N, Yousefi R, Jaganathan A, et al. (2018) Absolute and relative facial selectivities in organocatalytic asymmetric chlorocyclization reactions. Chemical Science. 9: 2898-2908 |
Soltanzadeh B, Jaganathan A, Yi Y, et al. (2017) Highly Regio- and Enantioselective Vicinal Dihalogenation of Allyl Amides. Journal of the American Chemical Society |
Li Z, Gelbaum C, Campbell ZS, et al. (2017) Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base New Journal of Chemistry. 41: 15420-15432 |
Li Z, Gelbaum C, Fisk JS, et al. (2016) Aqueous Suzuki Coupling Reactions of Basic Nitrogen-Containing Substrates in the Absence of Added Base and Ligand: Observation of High Yields under Acidic Conditions. The Journal of Organic Chemistry |
Li Z, Gelbaum C, Heaner WL, et al. (2016) Palladium-Catalyzed Suzuki Reactions in Water with No Added Ligand: Effects of Reaction Scale, Temperature, pH of Aqueous Phase, and Substrate Structure Organic Process Research & Development. 20: 1489-1499 |
Soltanzadeh B, Jaganathan A, Staples RJ, et al. (2015) Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides. Angewandte Chemie (International Ed. in English) |
Zhang C, Pan H, Klosin J, et al. (2015) Synthetic optimization and scale-up of imino-amido hafnium and zirconium olefin polymerization catalysts Organic Process Research and Development. 19: 1383-1391 |
Ashtekar KD, Marzijarani NS, Jaganathan A, et al. (2014) A new tool to guide halofunctionalization reactions: the halenium affinity (HalA) scale. Journal of the American Chemical Society. 136: 13355-62 |
Jaganathan A, Borhan B. (2014) Chlorosulfonamide salts are superior electrophilic chlorine precursors for the organocatalytic asymmetric chlorocyclization of unsaturated amides. Organic Letters. 16: 3616-9 |