DR
Dr B Janaki Ramulu
University of Southern California, Michigan State University, Osmania University, Indian Institute of Chemical Technology
Employment
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University of Southern California Research Lab Specialist2023 - Present
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Michigan State University Research Associate2021 - 2023
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Indian Institute of Chemical Technology Post-Doctoral Fellow2016 - 2021
Education
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Osmania University B.SC2003 - 2006
Projects & Funding
Projects & funding information is unavailable.
Publications (15)
- Catalyst-free one-pot four-component domino reactions in water-PEG-400: highly efficient and convergent approach to thiazoloquinoline scaffolds Save
- Lewis acid mediated three-component one-flask regioselective synthesis of densely functionalized 4-amino-1,2-dihydropyridines via cascade Knoevenagel/Michael/cyclization sequence Save
- Ligand- and Base-Free Cu-II-Mediated Selective S-Arylation of alpha-Enolic Dithioesters by Chan-Lam Coupling at Room Temperature Save
- Metal-Free Reagent Dependent S-S and C-C Homocoupling of alpha-Enolic Dithioesters at Room Temperature: Direct Access to Fully Substituted Symmetrical Thiophenes via Chemoselective Paal-Knorr Approach Save
- Organoindium mediated Csp(3)-S cross-coupling/migratory allenylation/thioannulation cascade: expedient synthesis of highly substituted thiophene frameworks Save
- A facile and straightforward synthesis of 1,2,3-thiadiazoles from alpha-enolicdithioesters via nitrosation/reduction/diazotization/cyclization cascade in one-pot Save
- Easy access to alpha-hydroxyimino-beta-oxodithioesters and application towards the synthesis of diverse 1,4-thiazine-3-ones via reduction/annulation cascade Save
- Indium(0)-Mediated C(sp)3-S/O Cross-Coupling Approach Towards the Regioselective Alkylation of alpha-Enolic Esters/Dithioesters: A Mechanistic Insight Save
- Iron-Promoted Domino Annulation of alpha-Enolic Dithioesters with Ninhydrin under Solvent-Free Conditions: Chemoselective Direct Access to Indeno[1,2-b]thiophenes Save
- Regioselective dehydrative intramolecular heteroannulation of beta-allyl-beta-hydroxy dithioesters: facile and straightforward entry to 2H-thiopyrans Save