[1]
Favre, H.A. Powell, W.H. Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013: Applications to Specific Classes of Compounds; The Royal Society of Chemistry: Cambridge, 2013, p. 691.
[2]
Tollens, B.; Wigand, P. Ueber den Penta-Erythrit, einen aus Formaldehyd und Acetaldehyd synthetisch hergestellten vierwerthigen Alkohol. Eur. J. Org. Chem., 1891, 265(3), 316-340.
[3]
Schurink, H.B.J. Pentaerythritol. Org. Synth., 1941, 1, 425.
[6]
Pani, B.; Sirohi, S.; Singh, D. Studies on the effects of various flame retardants on polypropylene. Am. J. Polym. Sci., 2013, 3(4), 63-69.
[8]
NPCS Board of Consultants & Engineers. The Complete Book on Adhesives, Glues & Resins Technology (with Process & Formulations), 2nd, Revised Edition; Asia Pacific Business Press Inc: Delhi, 2016.
[9]
NIIR Board of Engineers & Consultants. Synthetic Resins Technology Handbook; Asia Pacific Business Press Inc: Delhi, 2005.
[10]
Decato, S.; Bemis, T.; Madsen, E.; Mecozzi, S. Synthesis and characterization of perfluoro-tertbutyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery. Polym. Chem., 2014, 5(22), 6461-6471.
[11]
Marrian, S.F. The chemical reactions of pentaerythritol and its derivatives. Chem. Rev., 1948, 43(1), 149-202.
[12]
Barabanova, G.V.; Klimov, A.K.; Ivanov, V.I.; Kossova, L.V.; Vilenchuk, F.S.; Bebikh, G.F. Derivatives of 1,3-pyrimidine-thione (5,6-dihydro-2(1H)-pyrimidinethione) as additives for synthetic lubricating oils. Chem. Technol. Fuels Oils, 1980, 16(2), 780-782.
[13]
Nikonorov, E.M.; Sazonova, N.S.; Petrova, L.N.; Irisova, K.N.; Kalinina, E.V. Evaluation of thermal and thermal-oxidative stability of synthetic lubricants by derivatographic method. Chem. Technol. Fuels Oils, 1983, 19(4), 201-203.
[14]
Krakowiak, J. Densimetric and ultrasonic characterization of pentaerythritol in water and in aqueous NaCl and MgCl2 solutions at different temperatures. J. Chem. Thermodyn., 2012, 54, 444-452.
[15]
Venkitaraj, K.P.; Suresh, S. Experimental study on thermal and chemical stability of pentaerythritol blended with low melting alloy as possible pcm for latent heat storage. Exp. Therm. Fluid Sci., 2017, 88, 73-87.
[16]
Venkitaraj, K.P.; Suresh, S.; Venugopal, A. Experimental study on the thermal performance of nano enhanced pentaerythritol in IC engine exhaust heat recovery application. Appl. Therm. Eng., 2018, 137, 461-474.
[17]
Venkitaraj, K.P.; Suresh, S. Experimental study on the thermal storage performance and non-isothermal crystallization kinetics of pentaerythritol blended with low melting metal. Thermochim. Acta, 2018, 662, 75-89.
[18]
Mandrekar, V.K.; Chourasiya, G.; Kalsi, P.C.; Tilve, S.G.; Nadkarni, V.S. Nuclear track detection using thermoset polycarbonates derived from pentaerythritol. Nucl. Instrum. Methods Phys. Res. Sect. B., 2010, 268(5), 537-542.
[19]
Slough, W.; Perger, W.F. Application of an empirical dispersion potential to van der Waals binding in nitromethane, pentaerythritol, and pentaerythritol tetranitrate. Chem. Phys. Lett., 2010, 498(1-3), 97-100.
[20]
Trevoy, L.W.; Myers, M.E. Pentaerythritol derivatives: I. Mechanism of formation of dipentaerythritol. Can. J. Chem., 1963, 41(3), 770-776.
[21]
(a)Elibrocht, P.; Bärfacker, L.; Buss, C.; Hollmann, C.; Kitsos-Rzychon, B.E.; Kranemann, C.L.; Rische, T.; Roggenbuck, R.; Schmidt, A. Tandem reaction sequences under hydroformylation conditions: new synthetic applications of transition metal catalysis. Chem. Rev., 1999, 99(11), 3329-3366.
(b)Ugi, I. Recent progress in the chemistry of multicomponent reactions. Pure Appl. Chem., 2001, 73(1), 187-191.
(c)Simon, C.; Constantieux, T.; Rodriguez, J. Utilisation of 1,3‐dicarbonyl derivatives in multicomponent reactions. Eur. J. Org. Chem., 2004, 2004(24), 4957-4980.
(d)Hajipour, A.R.; Zarei, A.; Khazdooz, L.; Pourmousavi, S.A.; Zahmatkesh, S.; Ruoho, A.E. Efficient deprotection of tetrahydropyranyl ethers by silica sulfuric acid. Indian J. Chem. Sec. B, 2006, 45, 305-308.
[22]
Weber, L. The application of multi-component reactions in drug discovery. Curr. Med. Chem., 2002, 9(23), 2085-2093.
[23]
Padwa, A. Domino reactions of rhodium(II) carbenoids for alkaloid synthesis. Chem. Soc. Rev., 2009, 38(11), 3072-3081.
[24]
Rahman, O.U.; Bhat, S.I.; Yu, H.; Ahmad, S. Hyperbranched soya alkyd nanocomposite: a sustainable feedstock-based anticorrosive nanocomposite coatings. ACS Sustainable . Chem. Eng., 2017, 5(11), 9725-9734.
[25]
Fourcade, D.; Ritter, B.S.; Walter, P.; Schönfeld, R.; Mülhaupt, R. Renewable resource-based epoxy resins derived from multifunctional poly(4-hydroxybenzoates). Green Chem., 2013, 15(4), 910-918.
[26]
Chen, H.; Yu, B.; Jin, S. Production of levulinic acid from steam exploded rice straw via solid superacid, S2O82-/ZrO2–SiO2–Sm2O3. Bioresour. Technol., 2011, 102(3), 3568-3570.
[27]
Ji, H.; Wang, B.; Zhang, X.; Tan, T. Synthesis of levulinic acid-based polyol ester and its influence on tribological behavior as a potential lubricant. RSC Adv, 2015, 5(122), 100443-100451.
[28]
Wallace, K.J.; Hanes, R.; Anslyn, E.; Morey, J.; Kilway, K.V.; Siegel, J. Preparation of 1, 3, 5-tris (aminomethyl)-2, 4, 6-triethylbenzene from two versatile 1, 3, 5-tri (halosubstituted) 2, 4, 6-triethylbenzene derivatives. Synthesis, 2005, 2005(12), 2080-2083.
[29]
Içli, B.; Christinat, N.; Tönnemann, J.; Schüttler, C.; Scopelliti, R.; Severin, K. Synthesis of molecular nanostructures by multicomponent condensation reactions in a ball mill. J. Am. Chem. Soc., 2009, 131(9), 3154-3155.
[30]
Itsikson, T.M.; Kagan, L.K.; Zharova, E.Y.; Sudarikova, T.I.; Itsikson, L.B.; Nikonorov, E.M.; D’yakonova, K.D. Influence of catalyst on method of preparation and properties of pentaerythritol esters. Chem. Technol. Fuels Oils, 1975, 11(8), 594-596.
[31]
Bien, F.; Ziegler, T. Chemoenzymatic synthesis of glycosylated enantiomerically pure 4-pentene 1,2- and 1,3-diol derivatives. Tetrahedron Asymmmetry, 1998, 9(5), 781-790.
[32]
Lindhorst, T.K.; Dubber, M.; Krallmann-Wenzel, U.; Ehlers, S. Cluster mannosides as inhibitors of type 1 fimbriae-mediated adhesion of escherichia coli: pentaerythritol derivatives as scaffolds. Eur. J. Org. Chem., 2000, 2000(11), 2027-2034.
[33]
Ihre, H.; Hult, A.; Fréchet, J.M.; Gitsov, I. Double-stage convergent approach for the synthesis of functionalized dendritic aliphatic polyesters based on 2,2-bis(hydroxymethyl)propionic acid. Macromolecules, 1998, 31(13), 4061-4068.
[34]
Pant, C.S.; Wagh, R.M.; Nair, J.K.; Gore, G.M.; Thekkekara, M.; Venugopalan, S. Synthesis and Characterization of First Generation Dendritic Azidoesters. Propellants Explos. Pyrotech., 2007, 32(6), 461-467.
[35]
Abrishami, F.; Zarei, A.; Karegar, M. Synthesis of novel plasticizers based on poly(ε-caprolactone) and a consideration of their influence on nitroglycerine migration in double base solid propellants. Cent. Eur. J. Energ. Mater., 2018, 15(1), 150-161.
[36]
Sanchez, J.C.; Trogler, W.C. Polymerization of a boronate-functionalized fluorophore by double transesterification: applications to fluorescence detection of hydrogen peroxide vapor. J. Mater. Chem., 2008, 18(42), 5134-5141.
[37]
Issidorides, C.H.; Gulen, R.C. Monobenzalpentaerythritol. In: Organic Syntheses; Rabjohn, N., Ed.; John Wiley and Sons: New York, 1963; Collect. Vol. IV, pp. 679-681.
[38]
Garegg, P.J.; Johansson, R.; Ortega, C.; Samuelsson, B. Novel reagent system for converting a hydroxy-group into an iodogroup in carbohydrates with inversion of configuration. Part 3. J. Chem. Soc., Perkin Trans. 1, 1982, 681-683.
[39]
Lubineau, A.; Malleron, A.; Le Narvor, C. Chemo-enzymatic synthesis of oligosaccharides using a dendritic soluble support. Tetrahedron Lett., 2000, 41(46), 8887-8891.
[40]
Omura, K.; Swern, D. Oxidation of alcohols by “activated” dimethyl sulfoxide. A preparative, steric and mechanistic study. Tetrahedron, 1978, 34(11), 1651-1660.
[41]
Jahan, N.; Paul, N.; Petropolis, C.J.; Marangoni, D.G.; Grindley, T.B. Synthesis of surfactants based on pentaerythritol. i. cationic and zwitterionic gemini surfactants. J. Org. Chem., 2009, 74(20), 7762-7773.
[42]
Cheng, J.; Shi, W.; Zhang, L.; Zhang, R. A novel polyester composite nanofiltration membrane formed by interfacial polymerization of pentaerythritol (PE) and trimesoyl chloride (TMC). Appl. Surf. Sci., 2017, 416, 152-159.
[43]
a)Ben, T.; Pei, C.; Zhang, D.; Xu, J.; Deng, F.; Jing, X.; Qiu, S. Gas storage in porous aromatic frameworks (PAFs). Energy Environ. Sci., 2011, 4(10), 3991-3999.
(b)Rabbani, M.G.; El-Kaderi, H.M. Template-free synthesis of a highly porous benzimidazole-linked polymer for CO2 capture and H2 storage. Chem. Mater., 2011, 23(7), 1650-1653.
(c)Chen, Q.; Luo, M.; Hammershøj, P.; Zhou, D.; Han, Y.; Laursen, B.W.; Yan, C.G.; Han, B.H. Microporous polycarbazole with high specific surface area for gas storage and separation. J. Am. Chem. Soc., 2012, 134(14), 6084-6087.
(d)Zhao, Y.C.; Cheng, Q.Y.; Zhou, D.; Wang, T.; Han, B.H. Preparation and characterization of triptycene-based microporous poly(benzimidazole) networks. J. Mater. Chem., 2012, 22(23), 11509-11514.
(e)Wood, C.D.; Tan, B.; Trewin, A.; Su, F.; Rosseinsky, M.J.; Bradshaw, D.; Sun, Y.; Zhou, L.; Cooper, A.I. Microporous organic polymers for methane storage. Adv. Mater., 2008, 20(10), 1916-1921.
(f)Farha, O.K.; Bae, Y.S.; Hauser, B.G.; Spokoyny, A.M.; Snurr, R.Q.; Mirkin, C.A.; Hupp, J.T. Chemical reduction of a diimide based porous polymer for selective uptake of carbon dioxide versus methane. Chem. Commun. , 2010, 46(7), 1056-1058.
[44]
(a)Rakow, N.A.; Wendland, M.S.; Trend, J.E.; Poirier, R.J.; Paolucci, D.M.; Maki, S.P.; Lyons, C.S.; Swierczek, M.J. Visual indicator for trace organic volatiles. Langmuir, 2010, 26(6), 3767-3770.
(b)Liu, J.; Zong, E.; Fu, H.; Zheng, S.; Xu, Z.; Zhu, D. Adsorption of aromatic compounds on porous covalent triazine-based framework. J. Colloid Interface Sci., 2012, 372(1), 99-107.
(c)Rao, K.V.; Mohapatra, S.; Maji, T.K.; George, S.J. Guest-responsive reversible swelling and enhanced fluorescence in a super-absorbent, dynamic microporous polymer. Chem, 2012, 18(15), 4505-4509.
[45]
(a)Ding, S.Y.; Gao, J.; Wang, Q.; Zhang, Y.; Song, W.G.; Su, C.Y.; Wang, W. Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki-Miyaura coupling reaction. J. Am. Chem. Soc., 2011, 133(49), 19816-19822.
(b)Zhang, K.; Kopetzki, D.; Seeberger, P.H.; Antonietti, M.; Vilela, F. Surface area control and photocatalytic activity of conjugated microporous poly(benzothiadiazole) networks. Angew. Chem. Int. Ed., 2013, 52(5), 1432-1436.
[46]
McKeown, N.B.; Budd, P.M. Polymers of intrinsic microporosity (PIMs): organic materials for membrane separations, heterogeneous catalysis and hydrogen storage. Chem. Soc. Rev., 2006, 35(8), 675-683; (b) Budd, P.M.; McKeown, N.B. Highly permeable polymers for gas separation membranes. Polym. Chem., 2010, 1(1), 63-68.
[47]
Wolf, M.O.; Fox, H.H.; Fox, M.A. Reduction of acetylated tetraphenylethylenes: electrochemical behavior and stability of the related reduced anions. J. Org. Chem., 1996, 61(1), 287-294.
[48]
Li, H.; Ding, X.; Han, B-H. Tetraphenylethylene-based microporous organic polymers: insight into structure geometry, porosity, and CO2/CH4 selectivity. RSC Adv, 2016, 6(56), 51411-51418.
[49]
Zhao, Y.C.; Zhang, L.M.; Wang, T.; Han, B.H. Microporous organic polymers with acetal linkages: synthesis, characterization, and gas sorption properties. Polym. Chem., 2014, 5(2), 614-621.
[50]
Jana, T.; Koley, T.; Dhar, T.K. Effect of branching in hyperbranched alkyd on the performance of alkyd polyurethane coating. J. Appl. Polym. Sci., 2018, 135(9), 45835.
[51]
Wang, L.S.; Liu, Y.; Wang, R. Solubilities of some phosphaspirocyclic compounds in selected solvents. J. Chem. Eng. Data, 2006, 51(5), 1686-1689.
[52]
Zhang, P.; Zhang, Z.; Fan, H.; Tian, S.; Chen, Y.; Yan, J. Waterborne polyurethane conjugated with novel diol chain-extender bearing cyclic phosphoramidate lateral group: synthesis, flammability and thermal degradation mechanism. RSC Adv, 2016, 6(61), 56610-56622.
[53]
Wang, S.; Du, Z.; Cheng, X.; Liu, Y.; Wang, H. Synthesis of a phosphorus- and nitrogen-containing flame retardant and evaluation of its application in waterborne polyurethane. J. Appl. Polym. Sci., 2018, 135(16), 46093.
[54]
Padias, A.B.; Hall, Jr , H.K. Synthesis and polymerization of pentaerythritol monoacrylate and methacrylate and their bicyclic ortho esters. Macromolecules, 1982, 15(2), 217-223.
[55]
Stetsyshyn, Y.; Fornal, K.; Raczkowska, J.; Zemla, J.; Kostruba, A.; Ohar, H.; Ohar, M.; Donchak, V.; Harhay, K.; Awsiuk, K.; Rysz, J.; Bernasik, A.; Budkowski, A. Temperature and pH dual-responsive POEGMA-based coatings for protein adsorption. J. Colloid Interface Sci., 2013, 411, 247-256.
[56]
Stetsyshyn, Y.; Zemla, J.; Zolobko, O.; Fornal, K.; Budkowski, A.; Kostruba, A.; Donchak, V.; Harhay, K.; Awsiuk, K.; Rysz, J.; Bernasik, A.; Voronov, S. Temperature and pH dual-responsive coatings of oligoperoxide-graf t-poly(N-isopropylacrylamide): Wettability, morphology, and protein adsorption. J. Colloid Interface Sci., 2012, 387(1), 95-105.
[57]
Kostruba, A.; Ohar, M.; Kulyk, B.; Zolobko, O.; Stetsyshyn, Y. Surface modification by grafted sensitive polymer brushes: An ellipsometric study of their properties. Appl. Surf. Sci., 2013, 276, 340-346.
[58]
Stetsyshyn, Y.; Raczkowska, J.; Budkowski, A.; Kostruba, A. Harhay, Harhay, K.; Ohar, H.; Awsiuk, K.; Bernasik, A.; Ripak, N.; Zemła, J. Synthesis and postpolymerization modification of thermoresponsive coatings based on pentaerythritol monomethacrylate: surface analysis, wettability, and protein adsorption. Langmuir, 2015, 31(35), 9675-9683.
[59]
Grajewski, J.; Piotrowska, K.; Zgorzelak, M.; Janiak, A.; Biniek-Antosiak, K.; Rychlewska, U.; Gawronski, J. Introduction of axial chirality at a spiro carbon atom in the synthesis of pentaerythritol-imine macrocycles. Org. Biomol. Chem., 2018, 16, 981-987.
[60]
Celis, N.A.; Godoy-Alcántar, C.; Guerrero-Álvarez, J.; Barba, V. Boron macrocycles based on multicomponent assemblies using (3-aminophenyl)boronic acid and pentaerythritol as common reagents; molecular receptors toward lewis bases. Eur. J. Inorg. Chem., 2014, 2014(9), 1477-1484.
[61]
Cruz-Huerta, J.; Salazar-Mendoza, D.; Hernández-Paredes, J.; Ahuactzic, I.F.H.; Höpfl, H. N-containing boronic esters as self-complementary building blocks for the assembly of 2D and 3D molecular networks. Chem. Commun. , 2012, 48(35), 4241-4243.
[62]
Christinat, N.; Scopelliti, R.; Severin, K. Multicomponent assembly of boronic acid based macrocycles and cages. Angew. Chem., 2008, 120(10), 1874-1878.
[63]
Makhseed, S.; McKeown, N.B. Novel spiro-polymers with enhanced solubility. Chem. Commun. , 1999, 255-256.
[64]
Sandler, S.R.; Karo, W. Polymer syntheses; Academic Press Inc: London, 1977, Vol. 2, p. 196.
[65]
Abdel-Razik, H.H.; El-Bahy, Z.M. Nanoporous materials based on spiroketal and spirothioketal polymers for separating methanol-toluene mixture. Chin. J. Polym. Sci., 2011, 29(4), 450-455.
[66]
Firouzabadi, H.; Iranpoor, N.; Hazarkhani, H. New applications of solid silica chloride (sio2-cl) in organic synthesis. Efficient preparation of diacetals of 2,2-bis(hydroxymethyl)-1,3-propanediol from different substrates and their transthioacetalization reactions. efficient regeneration of carbonyl compounds from acetals and acylals. Phosphorus Sulfur Silicon Relat. Elem., 2002, 177(12), 2847-2858.
[67]
Jin, T-S.; Wang, H-X.; Wang, K-F.; Li, T-S. Synthesis of diacetals from aldehydes and ketones with pentaerythritol catalyzed by silica sulfate under microwave irradiation. Synth. Commun., 2004, 34(16), 2993-2999.
[68]
Kim, S.J.; Bang, E.K.; Kim, B.H. Synthesis of novel phosphoramidite building blocks from pentaerythritol. Synlett, 2003, 2003(12), 1838-1840.
[69]
Ueno, Y.; Takeba, M.; Mikawa, M.; Matsuda, A. Nucleosides and Nucleotides. 182. Synthesis of Branched Oligodeoxynucleotides with Pentaerythritol at the Branch Point and Their Thermal Stabilization of Triplex Formation1. J. Org. Chem., 1999, 64(4), 1211-1217.
[70]
Liu, J.; Cui, S.; Li, Z.; Xu, S.; Xu, J.; Pan, X.; Liu, Y.; Dong, H.; Sun, H.; Guo, K. Polymerization of trimethylene carbonates using organic phosphoric acids. Polym. Chem., 2016, 7(35), 5526-5535.
[71]
Tang, X.; Gao, L.; Han, N.; Fan, X.; Zhou, Q. Synthesis and characterization of 4‐arm star side‐chain liquid crystalline polymers containing azobenzene with different terminal substituents via ATRP. J. Polym. Sci.Part A Polym. Chem., 2007, 45(15), 3342-3348.
[72]
Li, J.; Shi, L.; An, Y.; Li, Y.; Chen, X.; Dong, H. Reverse micelles of star-block copolymer as nanoreactors for preparation of gold nanoparticles. Polymer , 2006, 47(26), 8480-8487.
[73]
Luo, X.; Wang, G.; Pang, X.; Huang, J. Synthesis of a novel kind of amphiphilic graft copolymer with miktoarm star-shaped side chains. Macromolecules, 2008, 41(7), 2315-2317.
[74]
Wang, G.; Huang, J. Preparation of star‐shaped abc copolymers of polystyrene‐poly (ethylene oxide)‐polyglycidol using ethoxyethyl glycidyl ether as the cap molecule. Macromol. Rapid Commun., 2007, 28(3), 298-304.
[75]
Wang, G.; Luo, X.; Zhang, Y.; Huang, J. Synthesis of dendrimer-like copolymers based on the star[polystyrene-poly(ethylene oxide)-poly(ethoxyethyl glycidyl ether)] terpolymers by click chemistry. J. Polym. Sci.Part A Polym. Chem., 2009, 47(18), 4800-4810.
[76]
Organikum, 15th ed; VEB: Berlin, 1984, p. 490.
[77]
Nutaitis, C.F.; Gribble, G.W. Reactions of sodium borohydride in acidic media. xiv. reductive cleavage of cyclic acetals and ketals to hydroxyalkyl ethers. Org. Prep. Proced. Int., 1985, 17(1), 11-16.
[78]
Pegenau, A.; Hegmann, T.; Tschierske, C.; Diele, S. The importance of micro segregation for mesophase formation: thermotropic columnar mesophases of tetrahedral and other low-aspect-ratio organic materials. Chem. Eur. J., 1999, 5(5), 1643-1660.
[79]
Wang, G.; Fan, X.; Hu, B.; Zhang, Y.; Huang, J. Synthesis of eight-shaped poly(ethylene oxide) by the combination of glaser coupling with ring-opening polymerization. Macromol. Rapid Commun., 2011, 32(20), 1658-1663.
[80]
(a)Enhsen, A.; Kramer, W.; Wess, G. Bile acids in drug discovery. Drug Discovery . Today, 1998, 3(9), 409-418.
(b)Mukhopadhyay, S.; Maitra, U. Chemistry and biology of bile acids. Curr. Sci., 2004, 87(12), 1666-1683.
(c)Hofmann, A.F.; Hagey, L.R. Bile acids: Chemistry, pathochemistry, biology, pathobiology, and therapeutics. Cell. Mol. Life Sci., 2008, 65(16), 2461-2483.
[81]
(a)Tamminen, J.; Kolehmainen, E. Bile acids as building blocks of supramolecular hosts. Molecules, 2001, 6(1), 21-46.
(b)Virtanen, E.; Kolehmainen, E. Use of bile acids in pharmacological and supramolecular applications. Eur. J. Org. Chem., 2004, 2004(16), 3385-3399.
(c)Davis, A.P. Bile acid scaffolds in supramolecular chemistry: the interplay of design and synthesis. Molecules, 2007, 12(9), 2106-2122.
(d)Maitra, U. Unlocking the potential of bile acids in synthesis, supramolecular/materials chemistry and nanoscience. Org. Biomol. Chem., 2008, 6(4), 657-669.
[82]
Fieser, L.F.; Rajagopalan, S. Oxidation of Steroids. III. Selective Oxidations and Acylations in the Bile Acid Series1. J. Am. Chem. Soc., 1950, 72(12), 5530-5536.
[83]
Tochtrop, G.P.; DeKoster, G.T.; Cistola, D.P.; Covey, D.F. Synthesis of [3,4-13C2]-enriched bile salts as NMR probes of protein-ligand interactions. J. Org. Chem., 2002, 67(19), 6764-6771.
[84]
Ikonen, S.; Valkonen, A.; Juvonen, R.; Salo, H.; Kolehmainen, E. Bile acid-derived mono- and diketals—synthesis, structural characterization and self-assembling properties. Org. Biomol. Chem., 2010, 8(12), 2784-2794.
[85]
Huang, G.L.; Mei, X.Y.; Liu, M.X. Synthesis of (R)-2,3-epoxypropyl (1→3)-β-d-pentaglucoside. Carbohydr. Res., 2005, 340(4), 603-608.
[86]
Smith, A.; Nobmann, P.; Henehan, G.; Bourke, P.; Dunne, J. Synthesis and antimicrobial evaluation of carbohydrate and polyhydroxylated non-carbohydrate fatty acid ester and ether derivatives. Carbohydr. Res., 2008, 343(15), 2557-2566.
[87]
(a)Hanessian, S.; Prabhanjan, H.; Qiu, D.; Nambiar, S. Synthesis of chemically and functionally diverse scaffolds from pentaerythritol. Can. J. Chem., 1996, 74(9), 1731-1737.
(b)Hanessian, S.; Qiu, D.; Prabhanjan, H.; Reddy, G.V.; Lou, B. Synthesis of clustered D-GalNAc (Tn) and D-Galβ (1→3) GalNAc (T) antigenic motifs using a pentaerythritol scaffold. Can. J. Chem., 1996, 74(9), 1738-1747.
(c)Lindhorst, T.K.; Dubber, M.; Krallman-Wenzel, U.; Ehlers, S. Cluster mannosides as inhibitors of type 1 fimbriae‐mediated adhesion of escherichia coli: pentaerythritol derivatives as scaffolds. Eur. J. Org. Chem., 2000, 2000(11), 2027-2034.
(d)Ueno, Y.; Takeba, M.; Mikawa, M.; Matsuda, A. Nucleosides and nucleotides. 182. synthesis of branched oligodeoxynucleotides with pentaerythritol at the branch point and their thermal stabilization of triplex formation1. J. Org. Chem., 1999, 64(4), 1211-1217.
(e)Schmidt, M.; Dobner, B.; Nuhn, P. Synthesis of polyfunctional pentaerythritol-derivatives using a novel protective group strategy for the preparation of cluster-glycolipids. Synlett, 2000, 2000(8), 1157-1159.
[88]
David, S. The anomalous reactivity of the bis(dibutylstannylene)acetal of pentaerythritol: a case of triple activation. Carbohydr. Res., 2001, 331(3), 327-329.
[89]
Gulyás, H.; Dobó, A.; Bakos, J. Synthesis of sulfated mono- and ditertiary phosphines, complex chemistry and catalysis. Can. J. Chem., 2001, 79(5-6), 1040-1048.
[90]
Tran, T.; Jahan, N.; Marangoni, D.G.; Grindley, T.B. Synthesis of surfactants based on pentaerythritol. II. Anionic gemini surfactants. Can. J. Chem., 2013, 91(11), 1085-1092.
[91]
Saucier, M.; Sauriol, C.; Salvador, R.L. Amélioration de la synthèse des di-et tri-bromhydrines du pentaérythritol. Can. J. Chem., 1966, 44(13), 1599-1601.
[92]
Beyaert, M.; Govaert, F. Proc. Acad. Sci. Amsterdam, 1939, 42, 776-789.
[93]
Mckay, A.F.; Buchanan, M.N.; Grant, G.A. The reaction of primary amines with 2-nitramino-Δ2-1, 3-diazacycloalkenes. J. Am. Chem. Soc., 1949, 71(3), 766-770.
[94]
Bradbury, R.B.; Hancox, N.C.; Hatt, H.H. 261. The reaction between acetone and ammonia: the formation of pyrimidine compounds analogous to the aldoxans of späth. J. Chem. Soc., 1947, 1394-1399.
[95]
Salvador, R.L.; Saucier, M. Spirocyclic tetrahydropyrimidines derived from pentaerythritol. Can. J. Chem., 1968, 46(5), 751-755.
[96]
David, S.; Thiéffry, A.; Veyrières, A. A mild procedure for the regiospecific benzylation and allylation of polyhydroxy-compounds via their stannylene derivatives in non-polar solvents. J. Chem. Soc., Perkin Trans. 1, 1981, 1796-1801.
[97]
Al-Mughaid, H.; Grindley, T.B. Syntheses of monohydroxy benzyl ethers of polyols: tri-O-benzylpentaerythritol and other highly benzylated derivatives of symmetrical polyols. Carbohydr. Res., 2004, 339(15), 2607-2610.
[10]
Decato, S.; Bemis, T.; Madsen, E.; Mecozzi, S. Synthesis and characterization of perfluoro-tertbutyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery. Polym. Chem., 2014, 5(22), 6461-6471.
[98]
Findeis, R.A.; Gade, L.H. Tridentate phosphine ligands with novel linker-units. Dalton Trans., 2003, 249-254.
[99]
Findeis, R.A.; Gade, L.H. Tripodal phosphane ligands with novel linker units and their rhodium complexes as building blocks for dendrimer catalysts. Eur. J. Inorg. Chem., 2003, 2003(1), 99-110.
[100]
Padias, A.B.; Hall, Jr , H.K.; Tomalia, D.A. McConnell, J.R. Starburst Polyether Dendrimers. J. Org. Chem., 1987, 52(24), 5305-5312.
[101]
Röckendorf, N.; Sperling, O.; Lindhorst, T.K. Trivalent cluster mannosides with aromatic partial structure as ligands for the type 1 fimbrial lectin of Escherichia coli. Aust. J. Chem., 2002, 55(2), 87-93.
[102]
Al-Mughaid, H.; Grindley, T.B. Improved routes for the preparation of pentaerythritol mono-o-benzyl ether. Synth. Commun., 2006, 36(18), 2569-2575.
[103]
Dunn, T.J.; Neumann, W.L.; Rogic, M.M.; Woulfe, S.R. Versatile methods for the synthesis of differentially functionalized pentaerythritol amine derivatives. J. Org. Chem., 1990, 55(26), 6368-6373.
[104]
Jiang, Z.X.; Yu, Y.B. The design and synthesis of highly branched and spherically symmetric fluorinated oils and amphiles. Tetrahedron, 2007, 63(19), 3982-3988.
[105]
Wuts, P.G.M.; Greene, T.W. Protective Groups in Organic Synthesis; Wiley & Sons: New York, 1999.
[106]
Balakumar, V.; Aravind, A.; Baskaran, S. A highly regio-and chemoselective reductive cleavage of benzylidene acetals with EtAlCl2-Et3SiH. Synlett, 2004, 2004(4), 647-650.
[107]
Yue, X.; Taraban, M.B.; Hyland, L.L.; Yu, Y.B. Avoiding steric congestion in dendrimer growth through proportionate branching: A twist on da Vinci’s rule of tree branching. J. Org. Chem., 2012, 77(20), 8879-8887.
[108]
Sukegawa, T.; Sato, K.; Oyaizu, K.; Nishide, H. Efficient charge transport of a radical polyether/ SWCNT composite electrode for an organic radical battery with high charge-storage density. RSC Adv, 2015, 5(20), 15448-15452.
[109]
Chen, S.; He, H.; Tang, G.; Wu, B.; Ma, M.; Shi, Y.; Wang, X. Topological structure influences on the gel formation process and mechanical properties of Llysine based supramolecular gels. RSC Adv, 2015, 5(123), 101437-101443.
[110]
Sugai, N.; Heguri, H.; Ohta, K.; Meng, Q.; Yamamoto, T.; Tezuka, Y. Effective click construction of bridged-and spiro-multicyclic polymer topologies with tailored cyclic prepolymers (kyklo-telechelics). J. Am. Chem. Soc., 2010, 132(42), 14790-14802.
[111]
Oike, H.; Imamura, H.; Imaizumi, H.; Tezuka, Y. Tailored synthesis of branched and network polymer structures by electrostatic self-assembly and covalent fixation with telechelic poly (THF) having N-phenylpyrrolidinium salt groups. Macromolecules, 1999, 32(15), 4819-4825.
[112]
Ko, Y.S.; Yamamoto, T.; Tezuka, Y. Click construction of spiro- and bridged-quatrefoil polymer topologies with kyklo-telechelics having an azide group. Macromol. Rapid Commun., 2014, 35(4), 412-416.
[113]
Hanessian, S.; Prabhanjan, H.; Qiu, D.; Nambiar, S. Synthesis of chemically and functionally diverse scaffolds from pentaerythritol. Can. J. Chem., 1996, 74(9), 1731-1737.
[114]
Mollard, A.; Zharov, I. Tricarboranyl pentaerythritol-based building block. Inorg. Chem., 2006, 45(25), 10172-10179.
[115]
a)Burai, R.; Chatwichien, J.; McNaughton, B.R. A programmable “build–couple” approach to the synthesis of heterofunctionalized polyvalent molecules. Org. Biomol. Chem., 2011, 9(14), 5056-5058.
(b)Ribeiro-Viana, R.; García-Vallejo, J.J.; Collado, D.; Pérez-Inestrosa, E.; Bloem, K.; van Kooyk, Y.; Rojo, J. BODIPY-labeled DC-SIGN-targeting glycodendrons efficiently internalize and route to lysosomes in human dendritic cells. Biomacromolecules, 2012, 13(10), 3209-3219.
(c)Luczkowiak, J.; Muñoz, A.; Sanchez-Navarro, M.; Ribeiro-Viana, R.; Ginieis, A.; Illescas, B.M.; Martín, N.; Delgado, R.; Rojo, J. Glycofullerenes inhibit viral infection. Biomacromolecules, 2013, 14(2), 431-437.
(d)Ortega-Muñoz, M.; Lopez-Jaramillo, J.; Hernadez-Mateo, F.; Santoyo-Gonzalez, F. Synthesis of glyco‐silicas by Cu (I)‐catalyzed “click‐chemistry” and their applications in affinity chromatography. Adv. Synth. Catal., 2006, 348(16-17), 2410-2420.
(e)Ribeiro-Viana, R.; Sanchez-Navarro, M.; Luczkowiak, J.; Koeppe, J.R.; Delgado, R.; Rojo, J.; Davis, B.G. Virus-like glycodendrinanoparticles displaying quasi-equivalent nested polyvalency upon glycoprotein platforms potently block viral infection. Nature . Commun., 2012, 3, 1303.
[116]
Compain, P.; Decroocq, C.; Joosten, A.; Sousa, J. Rodr_guez-Lucena, D.; Butters, T.D.; Bertrand, J.; Clément, R.; Boinot, C.; Becq, F.; Norez, C. Rescue of functional cftr channels in cystic fibrosis: a dramatic multivalent effect using iminosugar cluster-based correctors. ChemBioChem, 2013, 14(15), 2050-2058.
[117]
Joosten, A.; Decroocq, C.; Sousa, J.; Schneider, J.P.; Etamé, E.; Bodlenner, A.; Butters, T.D.; Compain, P. A systematic investigation of iminosugar click clusters as pharmacological chaperones for the treatment of gaucher disease. ChemBioChem, 2014, 15(2), 309-319.
[118]
Papp, I.; Dernedde, J.; Enders, S.; Haag, R. Modular synthesis of multivalent glycoarchitectures and their unique selectin binding behavior. Chem. Commun. , 2008, (44), 5851-5853.
[119]
Joosten, A.; Schneider, J.P.; Lepage, M.L.; Tarnus, C.; Bodlenner, A.; Compain, P. A convergent strategy for the synthesis of second-generation iminosugar clusters using “clickable” trivalent dendrons. Eur. J. Org. Chem., 2014, 2014(9), 1866-1872.
[120]
Sun, P.; Jiang, Y.; Xie, G.; Du, X.; Hu, J. A room temperature supramolecular-based quartz crystal microbalance (QCM) methane gas sensor. Sens. Actuators B., 2009, 141(1), 104-108.
[121]
Jiang, W.; Nowosinski, K.; Löw, N.L.; Dzyuba, E.V.; Klautzsch, F.; Schäfer, A.; Huuskonen, J.; Rissanen, K.; Schalley, C.A. Chelate cooperativity and spacer length effects on the assembly thermodynamics and kinetics of divalent pseudorotaxanes. J. Am. Chem. Soc., 2012, 134(3), 1860-1868.
[122]
Biju, V.; Sudeep, P.K.; Thomas, K.G.; George, M.V.; Barazzouk, S.; Kamat, P.V. Clusters of bis-and tris-fullerenes. Langmuir, 2002, 18(5), 1831-1839.
[123]
Pemba, A.G.; Rostagno, M.; Lee, T.A.; Miller, S.A. Cyclic and spirocyclic polyacetal ethers from lignin-based aromatics. Polym. Chem., 2014, 5(9), 3214-3221.
[124]
Gillies, E.R.; Fréchet, J.M. Dendrimers and dendritic polymers in drug delivery. Drug Discov. Today, 2005, 10(1), 35-43.
[125]
Lee, C.C.; MacKay, J.A.; Fréchet, J.M.J.; Szoka, F.C. Designing dendrimers for biological applications. Nat. Biotechnol., 2005, 23(12), 1517-1526.
[126]
Van der Poll, D.G.; Kieler-Ferguson, H.M.; Floyd, W.C.; Guillaudeu, S.J.; Jerger, K.; Szoka, F.C.; Fréchet, J.M. Design, synthesis, and biological evaluation of a robust, biodegradable dendrimer. Bioconjugate . Chem., 2010, 21(4), 764-773.
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