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Ramesh Yella
Ramesh Yella
Chugai Pharma Endowment Researcher 🔹 Small Molecule Expert 🔹 Scientific Speaker 🔹 Network Builder
Verified email at fos.kuicr.kyoto-u.ac.jp - Homepage
Title
Cited by
Cited by
Year
Tandem regioselective synthesis of tetrazoles and related heterocycles using iodine
R Yella, N Khatun, SK Rout, BK Patel
Organic & Biomolecular Chemistry 9 (9), 3235-3245, 2011
882011
Desulfurization mediated by hypervalent iodine (III): A novel strategy for the construction of heterocycles
H Ghosh, R Yella, J Nath, BK Patel
European Journal of Organic Chemistry 2008 (36), 6189-6196, 2008
852008
One-pot synthesis of five and six membered N, O, S-heterocycles using a ditribromide reagent
R Yella, BK Patel
Journal of Combinatorial Chemistry 12 (5), 754-763, 2010
662010
It is “2-imino-4-thiazolidinones” and not thiohydantoins as the reaction product of 1, 3-disubstituted thioureas and chloroacetylchloride
R Yella, H Ghosh, BK Patel
Green Chemistry 10 (12), 1307-1312, 2008
572008
An efficient synthesis of cyanamide from amine promoted by a hypervalent iodine (III) reagent
H Ghosh, R Yella, AR Ali, SK Sahoo, BK Patel
Tetrahedron Letters 50 (20), 2407-2410, 2009
552009
Copper (I)‐Catalyzed Cascade Synthesis of 2‐Substituted 1, 3‐Benzothiazoles: Direct Access to Benzothiazolones
S Murru, P Mondal, R Yella, BK Patel
European Journal of Organic Chemistry 2009 (31), 5406-5413, 2009
512009
Molecular iodine mediated preparation of isothiocyanates from dithiocarbamic acid salts
J Nath, H Ghosh, R Yella, BK Patel
European Journal of Organic Chemistry 2009 (12), 1849-1851, 2009
372009
Efficient preparation of isothiocyanates from dithiocarbamates using bromineless brominating reagent
R Yella, H Ghosh, S Murru, SK Sahoo, BK Patel
Synthetic Communications® 40 (14), 2083-2096, 2010
272010
T3P®–A benign desulfurating reagent in the synthesis of isothiocyanates
Ł Janczewski, A Gajda, S Frankowski, TM Goszczyński, T Gajda
Synthesis 50 (05), 1141-1151, 2018
222018
Arylthioureas with bromine or its equivalents gives no ‘Hugerschoff’reaction product
R Yella, S Murru, AR Ali, BK Patel
Organic & Biomolecular Chemistry 8 (15), 3389-3393, 2010
182010
Efficient one-pot preparation of bis alkyl xanthogen disulfides from alcohols
L Jamir, R Yella, BK Patel
Journal of Sulfur Chemistry 30 (2), 128-134, 2009
162009
Reduction of 4-Styrylpyridine by SmI2: An Inner Sphere Electron Tranfer Case Where the Binding Site Differs from the Reaction Center
R Yella, S Hoz
Organic letters 15 (20), 5262-5265, 2013
122013
Bromineless bromine as an efficient desulfurizing agent for the preparation of cyanamides and 2-aminothiazoles from dithiocarbamate salts
R Yella, V Kavala, BK Patel
Synthetic Communications 41 (6), 792-805, 2011
112011
Channeling the SmI2 Reactions to the Radical Path: Radicals Resisting Reduction by SmI2
R Yella, S Hoz
Organic letters 16 (15), 3876-3879, 2014
82014
A [2 + 3] Reductive Cyclodimerization of Quinoline by SmI2
R Yella, HE Gottlieb, S Hoz
The Journal of Organic Chemistry 80 (17), 8929-8932, 2015
32015
It is ‘thiazolidine-2, 4-dione’and not thiohydantoins as the reaction product of monosubstituted thioureas and chloroacetylchloride
R Yella, RK Singh, G Majji, BK Patel
Journal of Sulfur Chemistry 33 (1), 43-47, 2012
22012
Chloroacetylchloride: A versatile reagent in heterocyclic synthesis
R Yella
Synlett 2010 (05), 835-836, 2010
12010
Newer strategies for the synthesis of heterocycles using thiophilic reagents
R Yella
Guwahati, 2010
2010
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