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R. A.  Joshi, Garud, D. R., Muthukrishnan, M., Joshi, R. R., and Gurjar, M. K., ?Convenient synthesis of the enantiomerically pure beta-blocker (S)-betaxolol using hydrolytic kinetic resolution?, Tetrahedron-Asymmetry, vol. 16, no. 23, pp. 3802-3806, 2005.\par \par M.  Muthukrishnan, Patil, P. S., More, S. V., and Joshi, R. A., ?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.\par \par M.  Muthukrishnan, More, S. V., Garud, D. R., Ramana, C. V., Joshi, R. R., and Joshi, R. A., ?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.\par \par M.  Muthukrishnan, Garud, D. R., Joshi, R. R., and Joshi, R. A., ?Concise synthesis of beta-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution?, Tetrahedron, vol. 63, no. 8, pp. 1872-1876, 2007.\par \par M.  Muthukrishnan and Singh, O. V., ?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.\par \par M.  Sasikumar, Nikalje, M. D., and Muthukrishnan, M., ?Convenient synthesis of enantiomerically pure (R)-mexiletine using hydrolytic kinetic resolution method?, Tetrahedron-Asymmetry, vol. 20, no. 24, pp. 2814-2817, 2009.\par \par M.  Muthukrishnan, Basavanag, U. M. V., and Puranik, V. G., ?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.\par \par M. D.  Nikalje, Sasikumar, M., and Muthukrishnan, M., ?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.\par \par M.  Muthukrishnan, Mujahid, M., Punitharasu, V., and Dnyaneshwar, D. A., ?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.\par \par M.  Muthukrishnan, Mujahid, M., Sasikumar, M., and Mujumdar, P., ?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.\par \par M.  Muthukrishnan, Mujahid, M., Yogeeswari, P., and Sriram, D., ?Syntheses and biological evaluation of new triazole-spirochromone conjugates as inhibitors of mycobacterium tuberculosis?, Tetrahedron Letters, vol. 52, no. 18, pp. 2387-2389, 2011.\par \par M.  Mujahid, Mujumdar, P., Sasikumar, M., Kunte, S. S., and Muthukrishnan, M., ?Alternate synthesis of enantiomerically pure levetiracetam (Keppra (R))?, Tetrahedron-Asymmetry, vol. 23, no. 20-21, pp. 1512-1515, 2012.\par \par M.  Mujahid and Muthukrishnan, M., ?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.\par \par M.  Mujahid, Gonnade, R. G., Yogeeswari, P., Sriram, D., and Muthukrishnan, M., ?Synthesis and antitubercular activity of amino alcohol fused spirochromone conjugates?, Bioorganic & Medicinal Chemistry Letters, vol. 23, no. 5, pp. 1416-1419, 2013.\par \par M.  Mujahid, Kunte, S. S., and Muthukrishnan, M., ?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.\par \par A.  Reddi, Mujahid, M., Sasikumar, M., and Muthukrishnan, M., ?New enantioselective synthesis of the anti-parkinson agent safinamide?, Synthesis-Stuttgart, vol. 46, no. 13, pp. 1751-1756, 2014.\par \par N.  Viswanadh, Velayudham, R., Jambu, S., Sasikumar, M., and Muthukrishnan, M., ?Chiral aziridine ring opening: facile synthesis of (R)-modletine and (R)-phenoxybenzamine hydrochloride?, Tetrahedron Letters, vol. 56, no. 38, pp. 5269-5271, 2015.\par \par R.  Vyas, Karthikeyan, M., Nainaru, G., and Muthukrishnan, M., ?Pharmacophore and docking based virtual screening of validated mycobacterium tuberculosis targets?, Combinatorial Chemistry & High Throughput Screening, vol. 18, no. 7, pp. 624-637, 2015.\par \par N.  Viswanadh, Mujumdar, P., Sasikumar, M., Kunte, S. S., and Muthukrishnan, M., ?Alternate synthesis of appetite suppressant (R)-2-benzylmorpholine employing Sharpless asymmetric epoxidation strategy?, Tetrahedron Letters, vol. 57, no. 8, pp. 861-863, 2016.\par \par M.  Mujahid, Mujumdar, P., Sasikumar, M., Deshmukh, S. P., and Muthukrishnan, M., ?Efficient synthesis of the opioid analgesic (R)-phenampromide via an aziridinium ion?, Tetrahedron-Asymmetry, vol. 28, no. 7, pp. 983-986, 2017.\par \par M.  Mujahid, Subramanian, J., Nalla, V., Sasikumar, M., Kunte, S. Sharad, and Muthukrishnan, M., ?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.\par \par C.  Kurapati, Muthukrishnan, M., V. Singh, O., and Gundla, R., ?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.\par \par V.  Nalla, Mujahid, M., Sasikumar, M., Mujumdar, P., and Muthukrishnan, M., ?Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine?, Arkivoc, 2023.\par \par }