Shape-persistent macrocycle with intraannular alkyl groups: some structural limits of discotic liquid crystals with an inverted structure

Scholarly Works

• Delost, M. D.; Njardarson, J. T. Comprehensive Heterocyclic Chemistry IV - Oxiranes and Oxirenes: Monocyclic. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 199–274. doi:10.1016/b978-0-12-409547-2.14758-4
• Sagandira, C. R.; Khasipo, A. Z.; Sagandira, M. B.; Watts, P. An overview of the synthetic routes to essential oral anti-diabetes drugs. Tetrahedron 2021, 96, 132378. doi:10.1016/j.tet.2021.132378
• Roy, T.; Ghosal, S.; Thimmakondu, V. S. Six Low-Lying Isomers of C11H8 Are Unidentified in the Laboratory-A Theoretical Study. The journal of physical chemistry. A 2021, 125, 4352–4364. doi:10.1021/acs.jpca.1c02247
• Zhang, M.; Xu, Z.; Shi, D. Cu(I)–N-heterocyclic carbene-catalyzed base free C–N bond formation of arylboronic acids with amines and azoles. Tetrahedron 2021, 79, 131861. doi:10.1016/j.tet.2020.131861
• Hou, H.-L.; Cardo, L.; Mancino, D.; Arnaiz, B.; Criado, A.; Prato, M. Electrochemically controlled cleavage of imine bonds on a graphene platform: towards new electro-responsive hybrids for drug release. Nanoscale 2020, 12, 23824–23830. doi:10.1039/d0nr04102e
• Zhang, L.; Jiang, L.; Guan, X.; Cai, L.; Wang, J.; Xiang, P.; Pan, J.; Hu, X. A facile method to synthesize vildagliptin. Journal of Chemical Research 2020, 45, 174751982096712–309. doi:10.1177/1747519820967123
• Štefane, B.; Brodnik‐Žugelj, H.; Grošelj, U.; Svete, J.; Požgan, F. Copper Catalysis in Organic Synthesis; Wiley, 2020; pp 119–151. doi:10.1002/9783527826445.ch7
• Krishnamurti, V.; Barrett, C.; Prakash, G. K. S. Emerging Fluorinated Motifs; Wiley, 2020; pp 477–549. doi:10.1002/9783527824342.ch17
• Kumar, P. H.; Kumar, L. J.; Pavithrra, G.; Rajasekaran, R.; Vijayakumar, V.; Karan, R.; Sarveswari, S. Design, synthesis and exploration of in silico α-amylase and α-glucosidase binding studies of pyrrolidine-appended quinoline-constrained compounds. Research on Chemical Intermediates 2020, 46, 1869–1880. doi:10.1007/s11164-019-04068-9
• Ota, K.; Kohno, S.; Yamashita, T.; Miura, A.; Kamaike, K.; Miyaoka, H. Total synthesis of squafosacin F: stereodivergent approach to mono-tetrahydrofuran acetogenins. RSC advances 2019, 9, 40368–40377. doi:10.1039/c9ra09762g
• Sidhartha, S. K.; Cinu, A. T. Strategically Placed Trifluoromethyl Substituent in the Realm of Antitubercular Drug Design. Current Drug Therapy 2019, 14, 114–123. doi:10.2174/1574885513666180906101732
• Mekni, N. H. Nucleophilic Vinyl/Allyl, CF3 and CF2α Perfluoroalkyl Groups Substitution and/or E1CB Elimination Reactions of Fluorine Atom(s) in Organofluorinated Compounds. Mini-Reviews in Organic Chemistry 2019, 16, 453–462. doi:10.2174/1570193x15666180626130042
• Jamain, Z.; Khairuddean, M.; Saidin, S. A. Synthesis and characterization of 1,4-phenylenediamine derivatives containing hydroxyl and cyclotriphosphazene as terminal group. Journal of Molecular Structure 2019, 1186, 293–302. doi:10.1016/j.molstruc.2019.02.013
• Mane, K. D.; Kamble, R. B.; Suryavanshi, G. A visible light mediated, metal and oxidant free highly efficient cross dehydrogenative coupling (CDC) reaction between quinoxalin-2(1H)-ones and ethers. New Journal of Chemistry 2019, 43, 7403–7408. doi:10.1039/c9nj00075e
• Ota, K.; Yamashita, T.; Kohno, S.; Miura, A.; Kamaike, K.; Miyaoka, H. Formal synthesis of cis-solamin: acid-catalyzed one-step construction of 2,5-disubstituted tetrahydrofuran. Organic & biomolecular chemistry 2018, 16, 3018–3025. doi:10.1039/c8ob00603b
• Nam, J.-S.; Park, S.-Y.; Lee, H.-J.; Lee, S.-O.; Jang, H.-L.; Rhee, Y. H. Correlation Between Acetogenin Content and Antiproliferative Activity of Pawpaw (Asimina triloba [L.] Dunal) Fruit Pulp Grown in Korea. Journal of food science 2018, 83, 1430–1435. doi:10.1111/1750-3841.14144
• Abdou, W. M.; Ganoub, N. A. F.; Ismail, M.; Sabry, E.; Barghash, R. F.; Geronikaki, A. Developing efficient protocols for synthesis, antiosteoarthritic, antiinflammatory assessments and docking studies of nitrogen-containing bisphosphonate derivatives. Arabian Journal of Chemistry 2017, 10, 1084–1097. doi:10.1016/j.arabjc.2016.02.019
• Makhafola, T. J.; Elgorashi, E.; McGaw, L. J.; Awouafack, M. D.; Verschaeve, L.; Eloff, J. N. Isolation and characterization of the compounds responsible for the antimutagenic activity of Combretum microphyllum (Combretaceae) leaf extracts. BMC complementary and alternative medicine 2017, 17, 446. doi:10.1186/s12906-017-1935-5
• Francis, D. Antimicrobials from Microbes. Bioresources and Bioprocess in Biotechnology; Springer Singapore, 2017; pp 291–326. doi:10.1007/978-981-10-4284-3_12
• Adachi, Y.; Kuniyoshi, K.; Matsubara, H. Phase-vanishing method applied to condensation reactions using TiCl 4. Journal of Fluorine Chemistry 2017, 197, 100–105. doi:10.1016/j.jfluchem.2017.02.009

Explore citations to this article at