biblio
, “Alternate synthesis of appetite suppressant (R)-2-benzylmorpholine employing Sharpless asymmetric epoxidation strategy”, Tetrahedron Letters, vol. 57, no. 8, pp. 861-863, 2016.
, “Alternate synthesis of enantiomerically pure levetiracetam (Keppra (R))”, Tetrahedron-Asymmetry, vol. 23, no. 20-21, pp. 1512-1515, 2012.
, “Chiral aziridine ring opening: facile synthesis of (R)-modletine and (R)-phenoxybenzamine hydrochloride”, Tetrahedron Letters, vol. 56, no. 38, pp. 5269-5271, 2015.
, “Concise synthesis of beta-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution”, Tetrahedron, vol. 63, no. 8, pp. 1872-1876, 2007.
, “Convenient synthesis of enantiomerically pure (R)-mexiletine using hydrolytic kinetic resolution method”, Tetrahedron-Asymmetry, vol. 20, no. 24, pp. 2814-2817, 2009.
, “Convenient synthesis of the enantiomerically pure beta-blocker (S)-betaxolol using hydrolytic kinetic resolution”, Tetrahedron-Asymmetry, vol. 16, no. 23, pp. 3802-3806, 2005.
, “Efficient synthesis of the opioid analgesic (R)-phenampromide via an aziridinium ion”, Tetrahedron-Asymmetry, vol. 28, no. 7, pp. 983-986, 2017.
, “Facile enantioselective synthesis of enantiomerically pure (R)-phenoxybenzamine hydrochloride using the hydrolytic kinetic resolution method”, Tetrahedron-Asymmetry, vol. 21, no. 23, pp. 2825-2829, 2010.
, “Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid”, Mendeleev Communications, vol. 15, no. 3, pp. 100-101, 2005.
, “First asymmetric synthesis of the antiepileptic drug lacosamide (Vimpat (R)) based on a hydrolytic kinetic resolution strategy”, Tetrahedron-Asymmetry, vol. 22, no. 12, pp. 1353-1357, 2011.
, “First ionic liquid-promoted Kabbe condensation reaction for an expeditious synthesis of privileged bis-spirochromanone scaffolds”, Tetrahedron Letters, vol. 50, no. 22, pp. 2643-2648, 2009.
, “New and efficient enantioselective synthesis of both enantiomers of the calcium channel blocker bepridil”, New Journal of Chemistry, vol. 41, no. 2, pp. 824-829, 2017.
, “New enantioselective synthesis of (S)-2-ethoxy-3-(4-hydroxyphenyl)Propanoic acid esters (EEHP and IEHP), useful pharmaceutical intermediates of PPAR agonists”, Tetrahedron Letters, vol. 55, no. 21, pp. 3223-3226, 2014.
, “New enantioselective synthesis of the anticonvulsant drug pregabalin (lyrica) based on a hydrolytic kinetic resolution method”, Chirality, vol. 25, no. 12, pp. 965-969, 2013.
, “New enantioselective synthesis of the anti-parkinson agent safinamide”, Synthesis-Stuttgart, vol. 46, no. 13, pp. 1751-1756, 2014.
, “Pharmacophore and docking based virtual screening of validated mycobacterium tuberculosis targets”, Combinatorial Chemistry & High Throughput Screening, vol. 18, no. 7, pp. 624-637, 2015.
, “Pictet-Spengler cyclization in room temperature ionic liquid: a convenient access to tetrahydro beta-carbolines”, Journal of Heterocyclic Chemistry, vol. 43, no. 3, pp. 767-772, 2006.
, “Simple and efficient synthesis of 2-Aryl-2,3-dihydroquinolin-4(1H)-ones using silica chloride as a new catalyst under solvent-free conditions”, Synthetic Communications, vol. 40, no. 9, p. PII 921000023, 2010.
, “Syntheses and biological evaluation of new triazole-spirochromone conjugates as inhibitors of mycobacterium tuberculosis”, Tetrahedron Letters, vol. 52, no. 18, pp. 2387-2389, 2011.
, “Synthesis and antitubercular activity of amino alcohol fused spirochromone conjugates”, Bioorganic & Medicinal Chemistry Letters, vol. 23, no. 5, pp. 1416-1419, 2013.
, “Thallium(III) p-tosylate mediated oxidative 2,3-aryl rearrangement: a new useful route to ipriflavone and its analogs”, Synthetic Communications, vol. 38, no. 22, pp. 3875-3883, 2008.
, “Thallium(III) p-tosylate-mediated oxidative [1,2] rearrangement of 2-naphthyl and 2-heteroarylchromanones”, Journal of Heterocyclic Chemistry, vol. 59, no. 1, pp. 172-177, 2022.