[1]
Hierholtzer, A.; Chatellard, L.; Kierans, M.; Akunna, J.C.; Collier, P.J. The impact and mode of action of phenolic compounds extracted from brown seaweed on mixed anaerobic microbial cultures. J. Appl. Microbiol., 2013, 114(4), 964-973. [http://dx.doi.org/10.1111/jam.12114]. [PMID: 23279323].
[2]
Criquet, J.; Rodriguez, E.M.; Allard, S.; Wellauer, S.; Salhi, E.; Joll, C.A.; von Gunten, U. Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts--Electrophilic aromatic substitution and oxidation. Water Res., 2015, 85, 476-486. [http://dx.doi.org/10.1016/j.watres.2015.08.051]. [PMID: 26379203].
[3]
Bangera, M.G.; Thomashow, L.S. Identification and characterization of a gene cluster for synthesis of the polyketide antibiotic 2,4-diacetylphloroglucinol from Pseudomonas fluorescens Q2-87. J. Bacteriol., 1999, 181(10), 3155-3163. [PMID: 10322017].
[4]
Singh, I.P.; Sidana, J.; Bansal, P.; Foley, W.J. Phloroglucinol compounds of therapeutic interest: global patent and technology status. Expert Opin. Ther. Pat., 2009, 19(6), 847-866. [http://dx.doi.org/10.1517/13543770902916614]. [PMID: 19473105].
[6]
Davidson, P.M.; Branden, A.L. Antimicrobial activity of non-halogenated phenolic compounds. J. Food Prot., 1981, 44(8), 623-632. [http://dx.doi.org/10.4315/0362-028X-44.8.623]. [PMID: 30836539].
[7]
Hakimelahi, G.H.; Moshfegh, A.A. The synthesis of polyfunctional aromatic ring systems. Structural analogues of phloroglucides, aranciamycin, cryptosporin and terramycin. Helv. Chim. Acta, 1981, 64(2), 599-609. [http://dx.doi.org/10.1002/hlca.19810640224].
[8]
Hwu, J.R.; Moshfegh, A.A.; Tsay, S-C.; Lin, C.C.; Tseng, W.N.; Azaripour, A.; Mottaghian, H.; Hakimelahi, G.H. Cephalosporin 3′-phloroglucide esters and 7-(phloroglucidamido) cephalosporins as novel antibacterial agents. J. Med. Chem., 1997, 40(21), 3434-3441. [http://dx.doi.org/10.1021/jm960810e]. [PMID: 9341918].
[9]
Khalafi‐Nezhad, A.; Rad, M.N.S.; Hakimelahi, G.H. Synthesis of polyfunctional aromatic ring systems (phloroglucide analogs) under microwave irradiation. Helv. Chim. Acta, 2003, 86(7), 2396-2403. [http://dx.doi.org/10.1002/hlca.200390192].
[10]
Moshfegh, A.A.; Badri, R.; Hojjatie, M.; Kaviani, M.; Naderi, B.; Nazmi, A.H. The Synthesis of 4, 11, 18, 25‐Tetrachloro [14] metacyclophane‐7, 14, 21, 28‐tetroi. Structural Analogues of Phloroglucides. Helv. Chim. Acta, 1982, 65(4), 1221-1228. [http://dx.doi.org/10.1002/hlca.19820650411].
[11]
Khalafi-Nezhad, A.; Parhami, A.; Bargebid, R.; Molazade, S.; Zare, A.; Foroughi, H. Silica sulfuric acid as mild and efficient catalyst for the preparation of poly-hydroxyl aromatic compounds under mild and heterogeneous conditions. Mol. Divers., 2011, 15(2), 373-381. [http://dx.doi.org/10.1007/s11030-011-9303-8]. [PMID: 21340681].
[12]
Lee, S-M.; Na, M-K.; An, R-B.; Min, B-S.; Lee, H-K. Antioxidant activity of two phloroglucinol derivatives from Dryopteris crassirhizoma. Biol. Pharm. Bull., 2003, 26(9), 1354-1356. [http://dx.doi.org/10.1248/bpb.26.1354]. [PMID: 12951487].
[13]
Rostamizadeh, S.; Zekri, N. An efficient method for the synthesis of some new and known polyhydroxyl aromatic compounds (trisphenols) under solvent-free conditions. Polycycl. Aromat. Compd., 2016, 36(4), 329-341. [http://dx.doi.org/10.1080/10406638.2014.980435].
[14]
Choudhary, D.; Paul, S.; Gupta, R.; Clark, J.H. Catalytic properties of several palladium complexes covalently anchored onto silica for the aerobic oxidation of alcohols. Green Chem., 2006, 8(5), 479-482. [http://dx.doi.org/10.1039/b601363e].
[15]
Melero, J.A.; van Grieken, R.; Morales, G. Advances in the synthesis and catalytic applications of organosulfonic-functionalized mesostructured materials. Chem. Rev., 2006, 106(9), 3790-3812. [http://dx.doi.org/10.1021/cr050994h]. [PMID: 16967921].
[16]
Karimi, B.; Zareyee, D. Design of a highly efficient and water-tolerant sulfonic acid nanoreactor based on tunable ordered porous silica for the von Pechmann reaction. Org. Lett., 2008, 10(18), 3989-3992. [http://dx.doi.org/10.1021/ol8013107]. [PMID: 18702496].
[17]
Van Rhijn, W.; De Vos, D.; Sels, B.; Bossaert, W. Sulfonic acid functionalised ordered mesoporous materials as catalysts for condensation and esterification reactions. Chem. Commun., 1998, (3), 317-318. [http://dx.doi.org/10.1039/a707462j].
[18]
Mbaraka, I.K.; Radu, D.R.; Lin, V.S-Y.; Shanks, B.H. Organosulfonic acid-functionalized mesoporous silicas for the esterification of fatty acid. J. Catal., 2003, 219(2), 329-336. [http://dx.doi.org/10.1016/S0021-9517(03)00193-3].
[19]
Parhami, A.; Khalafi-Nezhad, A.; Haghighi, S.M.; Bargebid, R.; Zare, A.; Moosavi-Zare, A.R. Silica supported boric tri-sulfuric anhydride as a novel and efficient catalyst for solvent-free synthesis of coumarins via Pechmann condensation. ARKIVOC, 2012, 9, 111-121.
[20]
Wayne, P. National committee for clinical laboratory standards. Performance standards for antimicrobial disc susceptibility testing, 2002, 12, 01-53.
[21]
Clinical, Institute LS. Reference method for broth dilution antifungal
susceptibility testing of yeasts. Approved Standard-Third Edition
M27-A3,, 2008, 28