Prabhakararao Tharra

2015 IIT Madras 
"Prabhakararao Tharra"
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Beeraiah Baire grad student 2015 IIT Madras
 (The Z-enoate Assisted Meyer-Schuster Rearrangement: An Approach for the Unconventional Function)
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Roy D, Tharra P, Baire B. (2022) An approach to functionalized carbazoles from -enoate propargylic alcohols. A unified total synthesis of -Me-carazostatin, -Me-carbazoquinocin C and -Me-lipocarbazole A4. Chemical Communications (Cambridge, England). 58: 10210-10213
Roy D, Tharra P, Baire B. (2021) An Approach for the Generation of γ-Propenylidene-γ-butenolides and Application to the Total Synthesis of Rubrolides. Organic Letters
Jeyakumar M, Sathya S, Gandhi S, et al. (2019) α-bisabolol β-D-fucopyranoside as a potential modulator of β-amyloid peptide induced neurotoxicity: An in vitro &in silico study. Bioorganic Chemistry. 88: 102935
Tharra P, Baire B. (2018) Regioselective Cyclization of (Indol-3-yl)pentyn-3-ols as an Approach to (Tetrahydro)carbazoles. Organic Letters. 20: 1118-1121
Roy D, Tharra P, Baire B. (2018) Intercepted Meyer-Schuster Rearrangements in Organic Synthesis Asian Journal of Organic Chemistry. 7: 1015-1032
Tharra P, Baire B. (2017) A coherent study on the Z-enoate assisted Meyer-Schuster rearrangement. Organic & Biomolecular Chemistry. 15: 5579-5584
Tharra P, Baire B. (2017) Unconventional Reactivity of (Z)-Enoate Propargylic Alcohols in the Presence of Acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 2014-2017
Gandhi S, Tharra P, Baire B. (2017) Ag(I)-Catalyzed Cyclizative Hydration of Alkynes and Propargylic Alcohols. A Mild Approach to 2-Acylfuran Derivatives Chemistryselect. 2: 1058-1062
Tharra P, Baire B. (2016) Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans. Chemical Communications (Cambridge, England). 52: 14290-14293
Tharra P, Baire B. (2016) The Z-enoate assisted, Meyer-Schuster rearrangement cascade: unconventional synthesis of α-arylenone esters. Chemical Communications (Cambridge, England). 52: 12147-12150
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