Hari Prasad Kokatla

Affiliations: 
2013- NIT Warangal  
Area:
Organic synthesis, Carbohydrates, Medicinal Chemistry.
Website:
https://www.nitw.ac.in/faculty/id/16585/
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"Hari Prasad Kokatla"
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Publications

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Golla S, Poshala S, Pawar R, et al. (2020) Rongalite-promoted metal-free aerobic ipso-hydroxylation of arylboronic acids under sunlight: DFT mechanistic studies Tetrahedron Letters. 61: 151539
Beesu M, Kokatla HP, David SA. (2017) Syntheses of Human TLR8-Specific Small-Molecule Agonists. Methods in Molecular Biology (Clifton, N.J.). 1494: 29-44
Kokatla HP, Sil D, Tanji H, et al. (2014) Structure-based design of novel human Toll-like receptor 8 agonists. Chemmedchem. 9: 719-23
Kokatla HP, Sil D, Malladi SS, et al. (2013) Exquisite selectivity for human toll-like receptor 8 in substituted furo[2,3-c]quinolines. Journal of Medicinal Chemistry. 56: 6871-85
Kokatla HP, Yoo E, Salunke DB, et al. (2013) Toll-like receptor-8 agonistic activities in C2, C4, and C8 modified thiazolo[4,5-c]quinolines. Organic & Biomolecular Chemistry. 11: 1179-98
Kokatla HP, Lakshman MK. (2012) Two-step, one-pot synthesis of inosine, guanosine, and 2'-deoxyguanosine O6-ethers via intermediate O6-(benzotriazol-1-yl) derivatives. Current Protocols in Nucleic Acid Chemistry / Edited by Serge L. Beaucage ... [Et Al.]. Unit1.26
Kokatla HP, Thomson PF, Bae S, et al. (2011) Reduction of amine N-oxides by diboron reagents. The Journal of Organic Chemistry. 76: 7842-8
Lahiri R, Kokatla HP, Vankar YD. (2011) An improved method of ring closing metathesis in the presence of basic amines: application to the formal synthesis of (+)-lentiginosine and other piperidines and carbamino sugar analogs Tetrahedron Letters. 52: 781-786
Kokatla HP, Lakshman MK. (2010) One-pot etherification of purine nucleosides and pyrimidines. Organic Letters. 12: 4478-81
Kokatla HP, Lahiri R, Kancharla PK, et al. (2010) Synthesis of (-)-deoxoprosophylline, (+)-2-epi-deoxoprosopinine, and (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids from D-glycals. The Journal of Organic Chemistry. 75: 4608-11
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