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S. Prasad, Ganisetti, S., Jana, A., Kant, S., Sinha, P. K., Tripathy, S., Illath, K., Ajithkumar, T. G., Annapurna, K., Allu, A. R., and Biswas, K., “Elucidating the effect of CaF2 on structure, biocompatibility and antibacterial properties of S53P4 glass (vol 831, 154704, 2020)”, Journal of Alloys and Compounds, vol. 883, p. 161253, 2021.
A. P. Tathod and Dhepe, P. L., “Elucidating the effect of solid base on the hydrogenation of C5 and C6 sugars over Pt–Sn bimetallic catalyst at room temperature”, Carbohydrate Research, vol. 505, p. 108341, 2021.
S. R. Keshri, Mandal, I., Ganisetti, S., Kasimuthumaniyan, S., Kumar, R., Gaddam, A., Shelke, A., Ajithkumar, T. G., Gosvami, N. Nand, Krishnan, N. M. Anoop, and Allu, A. R., “Elucidating the influence of structure and Ag+ -Na+ ion-exchange on crack-resistance and ionic conductivity of Na3Al1.8Si1.65 P-1.8 O-12 glass electrolyte”, Acta Materialia, vol. 227, p. 117745, 2022.
P. Ghosh and Ghosha, D., “Elucidating the photoprotection mechanism of eumelanin monomers”, Journal of Physical Chemistry B, vol. 121, no. 24, pp. 5988-5994, 2017.
G. Rai and Kumar, A., “Elucidation of ionic interactions in the protic ionic liquid solutions by isothermal titration calorimetry”, Journal of Physical Chemistry B, vol. 118, no. 15, pp. 4160-4168, 2014.
V. Bhavnani, “Elucidation of molecular mechanism of stability of the heme-regulated eIF2α kinase upon binding of its ligand, hemin in its catalytic kinase domain”, Journal of Biomolecular Structure and Dynamics , vol. 35, pp. 1-17, 2017.
H. Singh, Bhagwat, S., Jouen, S., Lefez, B., Athawale, A. A., Hannoyer, B., and Ogale, S., “Elucidation of the role of hexamine and other precursors in the formation of magnetite nanorods and their stoichiometry”, Physical Chemistry Chemical Physics, vol. 12, no. 13, pp. 3246-3253, 2010.
K. Dinkar Sarode, V. Kumar, R., and Kulkarni, B. D., “Embedded multiple shooting methodology in a genetic algorithm framework for parameter estimation and state identification of complex systems”, Chemical Engineering Science, vol. 134, pp. 605-618, 2015.
K. Gupta, Jha, P. Kumar, Dadwal, A., Debnath, A. K., Jaiswal, I., Rana, S., Joy, P. A., and Ballav, N., “Embedding S=1/2 Kagome-like lattice in reduced graphene oxide”, Journal of Physical Chemistry Letters, vol. 10, no. 11, pp. 2663-2668, 2019.
A. Singh, Bhattacharyya, S. Maitra, and Singh, Y., “Emergence of cooperatively reorganizing cluster and super-Arrhenius dynamics of fragile supercooled liquids”, Physical Review E, vol. 103, no. 3, p. 032611, 2021.
C. Meena, Hens, C., Acharyya, S., Haber, S., Boccaletti, S., and Barzel, B., “Emergent stability in complex network dynamics”, Nature Physics, vol. 19, no. 7, p. 1033+, 2023.
D. J. Late, Rout, C. Sekhar, Chakravarty, D., and Ratha, S., “Emerging energy applications of two-dimensional layered materials”, Canadian Chemical Transactions, vol. 3, no. 2, pp. 118-157, 2015.
G. Panditrao, Bhowmick, R., Meena, C., and Sarkar, R. Rup, “Emerging landscape of molecular interaction networks: opportunities, challenges and prospects”, Journal of Biosciences, vol. 47, no. 2, p. 24, 2022.
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.
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.
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.
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.
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.
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.
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.
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.
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 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, 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.
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. 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.
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.
S. M. Inamdar, Shinde, V. S., and Patil, N. T., “Enantioselective cooperative catalysis”, Organic & Biomolecular Chemistry, vol. 13, no. 30, pp. 8116-8162, 2015.
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. 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.
A. Kumar Mutyala and Patil, N. T., “Enantioselective heterogeneous bronsted acid catalysis”, Organic Chemistry Frontiers, vol. 1, no. 5, pp. 582-586, 2014.
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.
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.
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. 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.
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. 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.
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 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.
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. 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.
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. 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.
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.
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. 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.
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.
P. Sarathi Chowdhury, Gupta, P., and Kumar, P., “Enantioselective synthesis of decarestrictine J”, Tetrahedron Letters, vol. 50, no. 51, pp. 7188-7190, 2009.
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.
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. 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.
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.
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.
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.
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.
V. S. Naidu and Kumar, P., “Enantioselective synthesis of (-)-pinellic acid”, Tetrahedron Letter, vol. 48, no. 13, pp. 2279-2282, 2007.
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. 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. A. Siddiqui and Srinivasan, K. V., “Enantioselective synthesis of (S)-dapoxetine”, Tetrahedron-Asymmetry, vol. 18, no. 17, pp. 2099-2103, 2007.
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. 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. 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. 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. 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.
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. George and Sudalai, A., “Enantioselective synthesis of tarchonanthuslactone using proline-catalyzed asymmetric alpha-aminooxylation”, Tetrahedron-Asymmetry, vol. 18, no. 8, pp. 975-981, 2007.
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. 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.
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.
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.
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.
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.
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.
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.
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., 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.
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.
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.
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.
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.
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.
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.
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. 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.
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.
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.
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.
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.
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.
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. 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.
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.
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.
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.
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.
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.
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.
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. 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. 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.

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