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M. Wahid, Puthusseri, D., Phase, D., and Ogale, S., Enhanced capacitance retention in a supercapacitor made of carbon from sugarcane bagasse by hydrothermal pretreatment, Energy & Fuels, vol. 28, no. 6, pp. 4233-4240, 2014.
P. Pandey, Seo, H. Hyun, Kim, H. - I., Ryu, S. Hwan, Dingre, M., Moh, S. Hyun, Kulkarni, A., and Parasharami, V. A., Enhanced anti-ageing and wound healing properties of Ficus religiosa L. bark, leaf and aerial root extract in human keratinocytes cell line (HaCaT), Vegetos, vol. 33, no. 1, pp. 158-165, 2020.
C. R. Patil, Niphadkar, P., Kamble, S. P., and V. Rode, C., Enhanced anisole hydroxylation over a hierarchical micro/mesoporous TS-1 catalyst, New Journal of Chemistry, vol. 46, no. 30, pp. 14667-14675, 2022.
S. Nahar, Nayak, A. K., Ghosh, A., Subudhi, U., and Maiti, S., Enhanced and synergistic downregulation of oncogenic miRNAs by self-assembled branched DNA, Nanoscale, vol. 10, no. 1, pp. 195-202, 2018.
S. Singh, Patel, K. A., Sonawane, P. D., Vishwakarma, R. K., and Khan, B. M., Enhanced activity of Withania somnifera family-1 glycosyltransferase (UGT73A16) via mutagenesis, World Journal Of Microbiology & Biotechnology, vol. 34, no. 10, 2018.
V. Amritkar, Adat, S., Tejwani, V., Rathore, A., and Bhambure, R., Engineering staphylococcal protein A for high-throughput affinity purification of monoclonal antibodies, Biotechnology Advances, vol. 44, p. 107632, 2020.
V. V. Ranade, Engineering reactors for catalytic reactions, Journal of Chemical Sciences, vol. 126, no. 2, pp. 341-351, 2014.
P. Panigrahi, Sule, M., Ghanate, A., Ramasamy, S., and Suresh, C. G., Engineering proteins for thermostability with iRDP web server, Plos One, vol. 10, no. 10, p. e0139486, 2015.
S. Gupta, Ciotonea, C., Royer, S., Dacquin, J. - P., and Vinod, C. P., Engineering pore morphology using silica template route over mesoporous cobalt oxide and its implications in atmospheric pressure carbon dioxide hydrogenation to olefins, vol. 19, p. 100586, 2020.
D. Ghosh and Ramasamy, S., Engineering of the tat pathway and chaperons, Acta Crystallographica A‐Foundation and Advances, vol. 70, p. C273, 2014.
A. Prabhu, Shanmugam, D., and Gadgil, M., Engineering nucleotide sugar synthesis pathways for independent and simultaneous modulation of N-glycan galactosylation and fucosylation in CHO cells, Metabolic Engineering, vol. 74, pp. 61-71, 2022.
S. Sharma, Thorat, S. H., Gonnade, R. G., Jasinski, J. P., Butcher, R., and Haridas, V., Engineering molecular topology: A pseudopeptidic macrocyclic figure-eight motif, European Journal of Organic Chemistry, no. 7, pp. 1120-1124, 2017.
A. M. Tamboli, Tamboli, M. S., Dwivedi, P. Kumari, Praveen, C. S., Karbhal, I., ,, Kim, B., Park, C., and Kale, B. B., Engineering microstructure of LiFe(MoO4)(2) as an advanced anode material for rechargeable lithium-ion battery, Journal of Materials Science-Materials In Electronics, vol. 32, no. 19, pp. 24273-24284, 2021.
S. M. Inamdar and Patil, N. T., Engineering ligands on the Au center: discovering broadly applicable gold catalysis with high turnover numbers, Organic Chemistry Frontiers, vol. 2, no. 8, pp. 995-998, 2015.
R. S. Barbole, Joshi, R. S., and Giri, A. P., Engineering inhibitory repeat domains of Pin-II type proteinase inhibitors indicate their high structural-functional tolerance to mutagenesis, Biochemical and Biophysical Research Communications, vol. 735, p. 150808, 2024.
M. I. Tamboli, Krishanaswamy, S., Gonnade, R. G., and Shashidhar, M. S., Engineering crystals that facilitate the acyl-transfer reaction: insight from a comparison of the crystal structures of myo-inositol-1,3,5-orthoformate-derived benzoates and carbonates, ACTA Crystallographica Section C-Structural Chemistry, vol. 72, no. 11, p. 875-+, 2016.
M. Gade, Chaudhary, P. Madhukar, Thulasiram, H. V., and Kikkeri, R., Engineering cell surface glycans with carbohydrate enantiomers to alter bacterial binding and adhesion, Chemistryselect, vol. 2, no. 28, pp. 8865-8869, 2017.
C. Ghosh, Gupta, N., More, P., Sengupta, P., Mallick, A., Santra, M. Kumar, and Basu, S., Engineering and in vitro evaluation of acid labile cholesterol tethered MG132 nanoparticle fortargeting ubiquitin-proteasome system in cancer, Chemistryselect, vol. 1, no. 16, pp. 5099-5106, 2016.
P. S. Giram, Nimma, R., Bulbule, A., Yadav, A. Singh, Gorain, M., Radharani, N. Naga Venka, Kundu, G. C., and Garnaik, B., Engineered PLGA core-lipid shell hybrid nanocarriers improve the efficacy and safety of irinotecan to combat colon cancer, ACS BIOMATERIALS SCIENCE & ENGINEERING, vol. 10, no. 10, pp. 6661-6676, 2024.
A. Tripathi, Singh, V., Aishwarya, K. G., Aradhyam, G. Krishna, and Hotha, S., Engineered glucose to generate a spectroscopic probe for studying carbohydrate biology, Advances in Experimental Medicine and Biology, vol. 749, pp. 313-327, 2012.
V. Nair, Menon, R. S., Sreekanth, A. R., Abhilash, N., and Biju, A. T., Engaging zwitterions in carbon-carbon and carbon-nitrogen bond- forming reactions: a promising synthetic strategy, Accounts of Chemical Research, vol. 39, no. 8, pp. 520–530, 2006.
T. Kaicharla, Yetra, S. Reddy, Roy, T., and Biju, A. T., Engaging isatins in solvent-free, sterically congested passerini reaction, Green Chemistry, vol. 15, no. 6, pp. 1608-1614, 2013.
P. K. Baruah, Sreedevi, N. K., Gonnade, R. G., Ravindranathan, S., Damodaran, K., Hofmann, H. - J., and Sanjayan, G. J., Enforcing periodic secondary structures in hybrid peptides: a novel hybrid foldamer containing periodic gamma-turn motifs, Journal of Organic Chemistry, vol. 72, no. 2, pp. 636-639, 2007.
T. V. Choudhary and Choudhary, V. R., Energy-efficient syngas production through, catalytic oxy-methane reforming reactions, Angewandte Chemie-International Edition, vol. 47, no. 10, pp. 1828-1847, 2008.
V. A. Pharande, Asthana, S. R., Saini, D. R., and Kaul, S. N., Energy optimization in integrated pulp and paper mills with recourse to environmental benefits, Journal of Scientific & Industrial Research, vol. 70, no. 12, pp. 1061-1069, 2011.
D. Dasgupta, Sidana, A., Ghosh, P., Sharma, T., Singh, J., Prabhune, A., More, S., Bhaskar, T., and Ghosh, D., Energy and life cycle impact assessment for xylitol production from corncob, Journal of Cleaner Production, vol. 278, p. 123217, 2021.
A. A. Al-Tabbakh, More, M. A., Joag, D. S., Ramgir, N. S., Mulla, I. S., and Pillai, V. K., Energy analysis of field emitted electrons from a ZnO tetrapod, Applied Physics Letters, vol. 90, no. 16, p. Article No. 162102, 2007.
G. Dadabhau Takalkar, Bhosale, R. R., Mali, N. A., and Bhagwat, S. S., Energetic and exergetic performance of NH3-H2O-based absorption refrigeration cycle: effect of operating factor, International Journal of Exergy, vol. 31, no. 4, pp. 352-369, 2020.
M. Varada, Erande, N. D., and Kumar, V. A., Ene-nucleic acids: a different paradigm to DNA chemistry, RSC Advances, vol. 5, no. 118, pp. 97824-97830, 2015.
D. Manzoor, Krishnamurty, S., and Pal, S., Endohedrally doped gold nanocages: efficient catalysts for O-2 activation and CO oxidation, Physical Chemistry Chemical Physics, vol. 18, no. 10, pp. 7068-7074, 2016.
M. Karthikeyan and Bender, A., Encoding and decoding graphical chemical structures as two-dimensional (PDF417) barcodes, Journal of Chemical Information and Modeling, vol. 45, no. 3, pp. 572-580, 2005.
A. Khan, Said, M. S., Borade, B. R., Gonnade, R., Barvkar, V., Kontham, R., and Dastager, S. G., Enceleamycins A-C, furo-naphthoquinones from amycolatopsis sp. MCC0218: isolation, structure elucidation, and antimicrobial activity, Journal of Natural Products, vol. 85, no. 5, pp. 1267-1273, 2022.
A. Chandralekha, A. Tavanandi, H., Amrutha, N., H. Hebbar, U., Raghavarao, K. S. M. S., and Gadre, R. V., Encapsulation of yeast (Saccharomyces cereviciae) by spray drying for extension of shelf life, Drying Technology, vol. 34, no. 11, pp. 1307-1318, 2016.
S. Mondal, Samanta, A., Dhar, B. B., and R. Devi, N., Encapsulation of ultra small metal clusters in silica: evolution of the concept of nanoreactors and the case of Ag-Pd@SiO2 alloy catalyst, Catalysis Today, vol. 251, pp. 114-120, 2015.
B. Malvi and Gupta, S. Sen, Encapsulation of enzyme in large mesoporous material with small mesoporous windows, Chemical Communications, vol. 48, no. 63, pp. 7853-7855, 2012.
A. Ramakrishnan, Pandit, N., Badgujar, M., Bhaskar, C., and Rao, M., Encapsulation of endoglucanase using a biopolymer Gum arabic for its controlled release, Bioresource Technology, vol. 98, no. 2, pp. 368-372, 2007.
A. K. Hajare, Datrange, L. S., Vyas, S., Bhuniya, D., and D. Reddy, S., Enantiospecific synthesis of sex pheromone of the obscure mealybug from pantolactone via tandem conjugate addition/cyclization, Tetrahedron Letters, vol. 51, no. 40, pp. 5291-5293, 2010.
R. Ramesh, Bell, V., Twidle, A. M., Gonnade, R. G., and D. Reddy, S., Enantiospecific synthesis of both enantiomers of the longtailed mealybug pheromone and their evaluation in a new zealand vineyard, Journal of Organic Chemistry, vol. 80, no. 15, pp. 7785-7789, 2015.
A. K. Hajare, Datrange, L. S., Murthy, Y. L. N., Bhuniya, D., and D. Reddy, S., Enantiospecific route to (+)-(1R, 3S)-cis-chrysanthemic acid from (-)-D-pantolactone(1), Synthesis-Stuttgart, no. 7, pp. 1067-1070, 2011.
P. R. Athawale, Kashinath, K., and D. Reddy, S., Enantiospecific formal synthesis of inthomycin C, Chemistry Select, vol. 1, no. 3, pp. 495–497, 2016.
P. Mondal and Argade, N. P., Enantioselective total synthesis of desbromoarborescidines A-C and the formal synthesis of (S)-deplancheine, Journal of Organic Chemistry, vol. 78, no. 13, pp. 6802-6808, 2013.
G. Pandey and Tiwari, D. Kumar, Enantioselective total synthesis of (2S,3R,4R)-D-xylo-phytosphingosine from substituted azetidin-2-one, Tetrahedron Letters, vol. 50, no. 26, pp. 3296-3298, 2009.
G. Pandey, Kumara, P. C., Burugu, S. Kumar, and Puranik, V. G., Enantioselective total syntheses of (-)-isonitramine, (-)-sibirine, and (+)-nitramine by ring-closing metathesis, European Journal of Organic Chemistry, no. 36, pp. 7372-7377, 2011.
S. Shee, Mukherjee, S., Gonnade, R. G., and Biju, A. T., Enantioselective synthesis of tricyclic beta-lactones by NHC-catalyzed desymmetrization of cyclic 1,3-diketones, Organic Letters, vol. 22, no. 14, pp. 5407-5411, 2020.
S. P. Chavan and Khatod, H. S., Enantioselective synthesis of the essential oil and pheromonal component ar-himachalene by a chiral pool and chirality induction approach, Tetrahedron-Asymmetry, vol. 23, no. 18-19, pp. 1410-1415, 2012.
P. Gupta, Naidu, S. V., and Kumar, P., Enantioselective synthesis of tarchonanthuslactone via iterative hydrolytic kinetic resolution, Tetrahedron Letters, vol. 46, no. 38, pp. 6571-6573, 2005.
S. George and Sudalai, A., Enantioselective synthesis of tarchonanthuslactone using proline-catalyzed asymmetric alpha-aminooxylation, Tetrahedron-Asymmetry, vol. 18, no. 8, pp. 975-981, 2007.
V. Jha, Kondekar, N. B., and Kumar, P., Enantioselective synthesis of syn/anti-1,3-amino alcohols via proline-catalyzed sequential alpha-aminoxylation/alpha-amination and horner-wadsworth-emmons olefination of aldehydes, Organic Letters, vol. 12, no. 12, pp. 2762-2765, 2010.
S. V. Narina and Sudalai, A., Enantioselective synthesis of (S)-timolol via kinetic resolution of terminal epoxides and dihydroxylation of allylamines, Tetrahedron, vol. 63, no. 14, pp. 3026-3030, 2007.
S. A. Siddiqui, Narkhede, U. C., Lahoti, R. J., and Srinivasan, K. V., Enantioselective synthesis of (+)-(S,S)-reboxetine, Synlett, no. 11, pp. 1771-1773, 2006.
S. P. Kotkar and Sudalai, A., Enantioselective synthesis of (S,S)-ethambutol using proline-catalyzed asymmetric alpha-aminooxylation and alpha-amination, Tetrahedron-Asymmetry, vol. 17, no. 11, pp. 1738-1742, 2006.
S. Reddy Yetra, Mondal, S., Mukherjee, S., Gonnade, R. G., and Biju, A. T., Enantioselective synthesis of spirocyclohexadienones by NHC-catalyzed formal [3+3] annulation reaction of enals, Angewandte Chemie-International Edition, vol. 55, no. 1, pp. 268-272, 2016.
S. Mukherjee, Joseph, S., Bhunia, A., Gonnade, R. Ghanshyam, Reddy, S. Vardhan, and Biju, A. T., Enantioselective synthesis of spiro γ-butyrolactones by N-heterocyclic carbene (NHC)-catalyzed formal [3+2] annulation of enals with 3-hydroxy oxindoles, Organic & Biomolecular Chemistry , vol. 16, pp. 2013 - 2019, 2017.
S. P. Bhoite and Suryavanshi, G., Enantioselective synthesis of (+)-Sedridine, (-)-Allosedridine and their N-Methyl analogs via Maruoka-Keck allylation and CBS reduction, Natural Product Research , vol. 37, no. 20, pp. 3388-3394, 2023.
S. A. Siddiqui and Srinivasan, K. V., Enantioselective synthesis of (S)-dapoxetine, Tetrahedron-Asymmetry, vol. 18, no. 17, pp. 2099-2103, 2007.
V. V. Thakur and Sudalai, A., Enantioselective synthesis of (S)-alpha-arylpropionic acids via pd-catalyzed kinetic resolution of benzylic alcohols, Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry, vol. 44, no. 3, pp. 557-562, 2005.
S. P. Panchgalle, Jogdand, G. F., Chavan, S. P., and Kalkote, U. R., Enantioselective synthesis of (R)-(+)-alpha-lipoic acid via proline-catalyzed sequential alpha-aminoxylation and HWE olefination of aldehyde, Tetrahedron Letters, vol. 51, no. 27, pp. 3587-3589, 2010.
V. S. Naidu and Kumar, P., Enantioselective synthesis of (-)-pinellic acid, Tetrahedron Letter, vol. 48, no. 13, pp. 2279-2282, 2007.
S. P. Bhoite, Kamble, R. B., and Suryavanshi, G. M., Enantioselective synthesis of (+)-hygroline and (+)-pseudohygroline via Keck allylation and CBS reduction, Tetrahedron Letters, vol. 56, no. 32, pp. 4704-4705, 2015.
S. K. Gadakh, R. Reddy, S., and Sudalai, A., Enantioselective synthesis of HIV protease inhibitor amprenavir via Co-catalyzed HKR of 2-(1-azido-2-phenylethyl)oxirane, Tetrahedron-Asymmetry, vol. 23, no. 11-12, pp. 898-903, 2012.
V. Venkataramasubramanian, B. Kumar, S., and Sudalai, A., Enantioselective synthesis of guggultetrol and D-ribo-phytosphingosine tetraacetate via L-proline catalyzed sequential alpha-aminooxylation/Horner-Wardsworth-Emmons olefination-Sharpless asymmetric dihydroxylation strategy, Tetrahedron-Asymmetry, vol. 26, no. 10-11, pp. 571-576, 2015.
E. K. Aratikatla, Kalamuddin, M., Malhotra, P., Mohmmed, A., and Bhattacharya, A. K., Enantioselective synthesis of gamma-phenyl-gamma-amino vinyl phosphonates and sulfones and their application to the synthesis of novel highly potent antimalarials, ACS Omega, vol. 5, no. 45, pp. 29025-29037, 2020.
S. Mondal, Mukherjee, S., Das, T. Kanti, Gonnade, R. G., and Biju, A. T., Enantioselective synthesis of functionalized β-lactones by NHC-catalyzed aldol lactonization of ketoacids, Journal of Organic Chemistry, vol. 82, no. 17, 2017.
S. Reddy Yetra, Mondal, S., Suresh, E., and Biju, A. T., Enantioselective synthesis of functionalized pyrazoles by NHC-catalyzed reaction of pyrazolones with alpha,beta-unsaturated aldehydes, Organic Letters, vol. 17, no. 6, pp. 1417-1420, 2015.
S. Barik, Shee, S., Gonnade, R. G., and Biju, A. T., Enantioselective synthesis of dihydrothiopyranones via NHC- catalyzed [3+3] annulation of 2-bromoenals with beta-oxodithioesters, Organic Letters, vol. 24, no. 48, pp. 8848-8853, 2022.
P. Sarathi Chowdhury, Gupta, P., and Kumar, P., Enantioselective synthesis of decarestrictine J, Tetrahedron Letters, vol. 50, no. 51, pp. 7188-7190, 2009.
S. V. Narina, Kumar, T. Siva, George, S., and Sudalai, A., Enantioselective synthesis of (-)-cytoxazone and (+)-epi-cytoxazone via Rh-catalyzed diastereoselective oxidative C-H aminations, Tetrahedron Letter, vol. 48, no. 1, pp. 65-68, 2007.
A. S. Paraskar and Sudalai, A., Enantioselective synthesis of (-)-cytoxazone and (+)-epi-cytoxazone, novel cytokine modulators via sharpless asymmetric epoxidation and L-proline catalyzed mannich reaction, Tetrahedron, vol. 62, no. 24, pp. 5756-5762, 2006.
T. Mahamadali Shaikh and Sudalai, A., Enantioselective synthesis of (+)-alpha-conhydrine and (-)-sedamine by L-proline-catalysed alpha-aminooxylation, European Journal of Organic Chemistry, no. 18, pp. 3437-3444, 2010.
A. Ghosh, Shee, S., Barik, S., Gonnade, R. G., and Biju, A. T., Enantioselective synthesis of 5,6-dihydroindolizines by N-heterocyclic carbene (NHC)-catalyzed core-structure-inspired strategy of azolium-enolate cascade, Organic Letters, vol. 23, no. 13, pp. 5223-5228, 2021.
S. Kumar Pandey and Kumar, P., Enantioselective synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine, Tetrahedron Letters, vol. 47, no. 25, pp. 4167-4169, 2006.
S. Bera, Enantioselective synthesis of 1-azaspiro[5.5]undecane ring system of histrionicotoxin alkaloids from D(+)-glucose, Heterocycles, vol. 65, no. 12, pp. 2901-2916, 2005.
S. P. Chavan, Khairnar, L. B., Pawar, K. P., Chavan, P. N., and Kawale, S. A., Enantioselective syntheses of (R)-pipecolic acid, (2R,3R)-3-hydroxypipecolic acid, beta-(+)-conhydrine and (-)-swainsonine using an aziridine derived common chiral synthon, RSC Advances, vol. 5, no. 62, pp. 50580-50590, 2015.
P. K. Baruah, Gonnade, R. G., and Sanjayan, G. J., Enantioselective syntheses of (-)-pinellic acid, alpha- and beta-dimorphecolic acid, Tetrahedron, vol. 63, no. 32, pp. 7624-7633, 2007.
S. B. Nikam and Asha, S. K., Enantioselective separation using chiral amino acid functionalized polyfluorene coated on mesoporous anodic aluminum oxide membranes (vol 92, pg 6850, 2020), Analytical Chemistry, vol. 93, no. 29, p. 10388, 2021.
S. B. Nikam and Asha, S. K., Enantioselective separation using chiral amino acid functionalized polyfluorene coated on mesoporous anodic aluminum oxide membranes, Analytical Chemistry, vol. 92, no. 10, pp. 6850-6857, 2020.
S. B. Nikam and K, A. S., Enantioselective separation of amino acids using chiral polystyrene microspheres synthesized by a post-polymer modification approach, ACS Polymers Au, vol. 2, no. 4, pp. 257–265, 2022.
H. S. Patil, Nikalje, M. D., Chopade, A. U., and Chopade, M. U., Enantioselective reduction of ketones and synthesis of 2-methyl-2,3-dihydro-1-benzofuran catalyzed by chiral spiroborate ester, Russian Journal of Organic Chemistry, vol. 57, no. 4, pp. 611-618, 2021.
S. Mukherjee, Shee, S., Poisson, T., Besset, T., and Biju, A. T., Enantioselective N-heterocyclic carbene-catalyzed cascade reaction for the synthesis of pyrroloquinolines via N-H functionalization of indoles, Organic letters , vol. 20, no. 22, pp. 6998-7002, 2018.
B. M. Sharma, Gontala, A., and Kumar, P., Enantioselective modular total synthesis of macrolides Sch725674 and C-4-epi-Sch725674, European Journal of Organic Chemistry, no. 6, pp. 1215-1226, 2016.
S. R. Sonavane and Mhaske, S. B., Enantioselective intramolecular decarboxylative C-H bond func-tionalization of quinazolinones with amino acids by visible light photoredox catalysis, Chemistry-An Asian Journal, vol. 18, no. 13, 2023.
S. Sahoo, Kumar, P., Lefebvre, F., and Halligudi, S. B., Enantioselective hydrogenation of olefins by chiral iridium phosphorothioite complex covalently anchored on mesoporous silica, Journal of Catalysis, vol. 254, no. 1, pp. 91-100, 2008.
A. Kumar Mutyala and Patil, N. T., Enantioselective heterogeneous bronsted acid catalysis, Organic Chemistry Frontiers, vol. 1, no. 5, pp. 582-586, 2014.
S. P. Chavan, Kadam, A. L., and Gonnade, R. G., Enantioselective formal total synthesis of (-)-quinagolide, Organic Letters, vol. 21, no. 22, pp. 9089-9093, 2019.
S. B. Jadhav, Dash, S. Ranjan, Maurya, S., Nanubolu, J. Babu, Vanka, K., and Chegondi, R., Enantioselective Cu(I)-catalyzed borylative cyclization of enone-tethered cyclohexadienones and mechanistic insights, Nature Communications, vol. 13, no. 1, p. 854, 2022.
S. M. Inamdar, Shinde, V. S., and Patil, N. T., Enantioselective cooperative catalysis, Organic & Biomolecular Chemistry, vol. 13, no. 30, pp. 8116-8162, 2015.
C. C. Chintawar, Bhoyare, V. W., Mane, M. V., and Patil, N. T., Enantioselective Au(I)/Au(III) redox catalysis enabled by chiral (P,N)-ligands, Journal of the American Chemical Society, vol. 144, no. 16, pp. 7089-7095, 2022.
P. D. Shinde, Jadhav, V. H., Borate, H. B., Bhide, S. R., Sonawane, K. B., and Wakharkar, R. D., Enantiomeric separation of novel anticancer agent 5-hydroxy-3-(4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-cyclopent-2-en- 1-one, Journal of Chromatography A, vol. 1138, no. 1-2, pp. 184-189, 2007.
B. M. Rajesh, Shinde, M. V., Kannan, M., Srinivas, G., Iqbal, J., and D. Reddy, S., Enantiodivergent routes to (+) and (-)-novioses from (-)-pantolactone, RSC Advances, vol. 3, no. 43, pp. 20291-20297, 2013.
P. Kumar, Pandey, M., Gupta, P., S. Naidu, V., and Dhavale, D. D., Enantio- and diastereocontrolled total synthesis of (+)-strictifolione, European Journal of Organic Chemistry, no. 36, pp. 6993-7004, 2010.
P. Kumar and Naidu, S. V., Enantio- and diastereocontrolled total synthesis of (+)-boronolide, Journal of Organic Chemistry, vol. 71, no. 10, pp. 3935-3941, 2006.
P. Kumar, Dubey, A., and Harbindu, A., Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (vol 10, pg 6987, 2012), Organic & Biomolecular Chemistry, vol. 18, no. 27, p. 5264, 2020.
P. Kumar, Dubey, A., and Harbindu, A., Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II, Organic & Biomolecular Chemistry, vol. 10, no. 34, pp. 6987-6994, 2012.
A. B. Lende, Dinker, M. K., Bhosale, V. K., Kamble, S. P., Meshram, P. D., and Kulkarni, P. S., Emulsion ionic liquid membranes (EILMs) for removal of Pb(II) from aqueous solutions, RSC Advances, vol. 4, no. 94, pp. 52316-52323, 2014.
V. Nair, Menon, R. S., Biju, A. T., Sinu, C. R., Paul, R. Rajan, Jose, A., and Sreekumar, V., Employing homoenolates generated by NHC catalysis in carbon-carbon bond-forming reactions: state of the art, Chemical Society Reviews, vol. 40, no. 11, pp. 5336-5346, 2011.
T. Roy, Bhojgude, S. Suresh, Kaicharla, T., Thangaraj, M., Garai, B., and Biju, A. T., Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines, Organic Chemistry Frontiers, vol. 3, no. 1, pp. 71-76, 2016.
A. Bhunia and Biju, A. T., Employing arynes in transition-metal-free, N-heterocycles initiated multicomponent reactions, Synlett, vol. 25, no. 5, pp. 608-614, 2014.
S. Suresh Bhojgude, Kaicharla, T., and Biju, A. T., Employing arynes in transition-metal-free monoarylation of aromatic tertiary amines, Organic Letters, vol. 15, no. 21, pp. 5452-5455, 2013.
S. Suresh Bhojgude, Bhunia, A., and Biju, A. T., Employing arynes in diels–alder reactions and transition-metal-free multicomponent coupling and arylation reactions, Accounts of Chemical Research, vol. 49, no. 9, pp. 1658-1670, 2016.
R. N. Gaykar, Bhunia, A., and Biju, A. T., Employing arynes for the generation of aryl anion equivalents and subsequent reaction with aldehydes, Journal of Organic Chemistry, vol. 83, no. 18, pp. 11333-11340, 2018.

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