메뉴 건너뛰기




Volumn 8, Issue 6, 2019, Pages

Synthesis of lipophilic esters of tyrosol, homovanillyl alcohol and hydroxytyrosol

Author keywords

Circular economy; Dimethyl carbonate; Green chemistry; Homovanillyl alcohol; Hydroxytyrosol; Hydroxytyrosol enriched extracts; Lipophilic alkyl esters; Olea europaea; Tyrosol

Indexed keywords


EID: 85068500020     PISSN: None     EISSN: 20763921     Source Type: Journal    
DOI: 10.3390/antiox8060174     Document Type: Article
Times cited : (25)

References (50)
  • 1
    • 34548444575 scopus 로고    scopus 로고
    • Phenolic molecules in virgin olive oils: A survey of their sensory properties, health effects, antioxidant activiy and analytical methods. An overview of the last decade
    • Bendini, A.; Cerretani, L.; Carrasco-Pancorbo, A.; Gomez-Caravaca, A.M.; Segura-Carretero, A.; Fernandez-Gutierrez, A.; Lercker, G. Phenolic molecules in virgin olive oils: A survey of their sensory properties, health effects, antioxidant activiy and analytical methods. An overview of the last decade. Molecules 2007, 12, 1679–1719. [CrossRef] [PubMed]
    • (2007) Molecules , vol.12 , pp. 1679-1719
    • Bendini, A.1    Cerretani, L.2    Carrasco-Pancorbo, A.3    Gomez-Caravaca, A.M.4    Segura-Carretero, A.5    Fernandez-Gutierrez, A.6    Lercker, G.7
  • 2
    • 2642527771 scopus 로고    scopus 로고
    • Low-molecular weight components of olive oil mill wastewaters
    • Della Greca, M.; Previtera, L.; Temussi, F.; Zarrelli, A. Low-molecular weight components of olive oil mill wastewaters. Phytochem. Anal. 2004, 15, 184–188. [CrossRef] [PubMed]
    • (2004) Phytochem. Anal. , vol.15 , pp. 184-188
    • della Greca, M.1    Previtera, L.2    Temussi, F.3    Zarrelli, A.4
  • 3
    • 84994803221 scopus 로고    scopus 로고
    • Sustainability, innovation and green chemistry in the production and valorization of phenolic extracts from Olea europaea L
    • Romani, A.; Pinelli, P.; Ieri, F.; Bernini, R. Sustainability, innovation and green chemistry in the production and valorization of phenolic extracts from Olea europaea L. Sustainability 2016, 8, 1002. [CrossRef]
    • (2016) Sustainability , vol.8 , pp. 1002
    • Romani, A.1    Pinelli, P.2    Ieri, F.3    Bernini, R.4
  • 4
    • 85027345826 scopus 로고    scopus 로고
    • Lipophilization of hydroxytyrosol-enriched fractions from Olea europaea L. By-products and evaluation of the in vitro effects on a model of colorectal cancer cells
    • Bernini, R.; Carastro, I.; Palmini, G.; Tanini, A.; Zonefrati, R.; Pinelli, P.; Brandi, M.L.; Romani, A. Lipophilization of hydroxytyrosol-enriched fractions from Olea europaea L. by-products and evaluation of the in vitro effects on a model of colorectal cancer cells. J. Agric. Food Chem. 2017, 65, 6506–6512. [CrossRef] [PubMed]
    • (2017) J. Agric. Food Chem. , vol.65 , pp. 6506-6512
    • Bernini, R.1    Carastro, I.2    Palmini, G.3    Tanini, A.4    Zonefrati, R.5    Pinelli, P.6    Brandi, M.L.7    Romani, A.8
  • 5
    • 84961658157 scopus 로고    scopus 로고
    • The circular economy
    • Stahel, W.R. The circular economy. Nature 2016, 531, 435–438. [CrossRef] [PubMed]
    • (2016) Nature , vol.531 , pp. 435-438
    • Stahel, W.R.1
  • 6
    • 85059267692 scopus 로고    scopus 로고
    • Protective role of polyphenols against vascular inflammation, aging and cardiovascular disease
    • Serino, A.; Salazar, G. Protective role of polyphenols against vascular inflammation, aging and cardiovascular disease. Nutrients 2019, 11, 53. [CrossRef]
    • (2019) Nutrients , vol.11 , pp. 53
    • Serino, A.1    Salazar, G.2
  • 8
    • 84935429527 scopus 로고    scopus 로고
    • Tyrosol suppresses allergic inflammation by inhibiting the activation of phosphoinositide 3-kinase in mast cells
    • In-Gyu Je, I.-G.; Kim, D.-S.; Kim, S.-W.; Lee, S.; Lee, H.-S.; Park, E.K.; Khang, D.; Kim, S.-H. Tyrosol suppresses allergic inflammation by inhibiting the activation of phosphoinositide 3-kinase in mast cells. PLoS ONE 2015. [CrossRef]
    • (2015) Plos ONE
    • In-Gyu Je, I.-G.1    Kim, D.-S.2    Kim, S.-W.3    Lee, S.4    Lee, H.-S.5    Park, E.K.6    Khang, D.7    Kim, S.-H.8
  • 10
    • 84892722585 scopus 로고    scopus 로고
    • Synthesis and DPPH radical scavenging activity of novel compounds obtained from tyrosol and cinnamic acid derivatives
    • Barontini, M.; Bernini, R.; Carastro, R.; Gentili, P.; Romani, A. Synthesis and DPPH radical scavenging activity of novel compounds obtained from tyrosol and cinnamic acid derivatives. New J. Chem. 2014, 38, 809–816. [CrossRef]
    • (2014) New J. Chem. , vol.38 , pp. 809-816
    • Barontini, M.1    Bernini, R.2    Carastro, R.3    Gentili, P.4    Romani, A.5
  • 11
    • 84964636286 scopus 로고    scopus 로고
    • Oxidative cleavage of 1-aryl-isochroman derivatives by the Trametes villosa laccase/1-hydroxybenzotroazole system
    • Bernini, R.; Crisante, F.; D’Acunzo, F.; Gentili, P.; Ussia, E. Oxidative cleavage of 1-aryl-isochroman derivatives by the Trametes villosa laccase/1-hydroxybenzotroazole system. New J. Chem. 2016, 40, 3314–3322. [CrossRef]
    • (2016) New J. Chem. , vol.40 , pp. 3314-3322
    • Bernini, R.1    Crisante, F.2    D’Acunzo, F.3    Gentili, P.4    Ussia, E.5
  • 12
    • 33847641037 scopus 로고    scopus 로고
    • Hydroxytyrosol lipophilic analogues: Enzymatic synthesis, radical scavenging activity and DNA oxidative damage protection
    • Grasso, S.; Siracusa, L.; Spatafora, C.; Renis, M.; Tringali, C. Hydroxytyrosol lipophilic analogues: enzymatic synthesis, radical scavenging activity and DNA oxidative damage protection. Bioorg. Chem. 2007, 35, 137–152. [CrossRef] [PubMed]
    • (2007) Bioorg. Chem. , vol.35 , pp. 137-152
    • Grasso, S.1    Siracusa, L.2    Spatafora, C.3    Renis, M.4    Tringali, C.5
  • 13
    • 85058476159 scopus 로고    scopus 로고
    • Biological relevance of extra virgin olive oil polyphenols metabolites
    • Serreli, G.; Deiana, M. Biological relevance of extra virgin olive oil polyphenols metabolites. Antioxidants 2018, 7, 170. [CrossRef] [PubMed]
    • (2018) Antioxidants , vol.7 , pp. 170
    • Serreli, G.1    Deiana, M.2
  • 14
    • 0037471582 scopus 로고    scopus 로고
    • Quantitative kinetic analysis of hydrogen transfer reactions from dietary polyphenols to the DPPH radical
    • Goupy, P.; Dufour, C.; Loonis, M.; Dangles, O. Quantitative kinetic analysis of hydrogen transfer reactions from dietary polyphenols to the DPPH radical. J. Agric. Food Chem. 2003, 51, 615–622. [CrossRef] [PubMed]
    • (2003) J. Agric. Food Chem. , vol.51 , pp. 615-622
    • Goupy, P.1    Dufour, C.2    Loonis, M.3    Dangles, O.4
  • 15
    • 84877979324 scopus 로고    scopus 로고
    • Naturally occurring hydroxytyrosol: Synthesis and anticancer potential
    • Bernini, R.; Merendino, N.; Romani, A.; Velotti, F. Naturally occurring hydroxytyrosol: Synthesis and anticancer potential. Curr. Med. Chem. 2013, 20, 655–670. [CrossRef] [PubMed]
    • (2013) Curr. Med. Chem. , vol.20 , pp. 655-670
    • Bernini, R.1    Merendino, N.2    Romani, A.3    Velotti, F.4
  • 16
    • 84949870604 scopus 로고    scopus 로고
    • Hydroxytyrosol-derived compounds: A basis for the creation of new pharmacological agents for cancer prevention and therapy
    • Bernini, R.; Gilardini Montani, M.S.; Merendino, N.; Romani, A. Velotti, F. Hydroxytyrosol-derived compounds: a basis for the creation of new pharmacological agents for cancer prevention and therapy. J. Med. Chem. 2015, 58, 9089–9107. [CrossRef] [PubMed]
    • (2015) J. Med. Chem. , vol.58 , pp. 9089-9107
    • Bernini, R.1    Gilardini Montani, M.S.2    Merendino, N.3    Romani, A.4    Velotti, F.5
  • 17
    • 85057746907 scopus 로고    scopus 로고
    • Hydroxytyrosol exerts anti-inflammatory and anti-oxidant activities in a mouse model of systemic inflammation
    • Fuccelli, R.; Fabiani, R.; Rosignoli, P. Hydroxytyrosol exerts anti-inflammatory and anti-oxidant activities in a mouse model of systemic inflammation. Molecules 2018, 23, 3212. [CrossRef] [PubMed]
    • (2018) Molecules , vol.23 , pp. 3212
    • Fuccelli, R.1    Fabiani, R.2    Rosignoli, P.3
  • 18
    • 85062856245 scopus 로고    scopus 로고
    • Hydroxytyrosol protects from aging process via AMPK and autophagy; a review of its effects on cancer, metabolic syndrome, osteoporosis, immune-mediated and neurodegenerative diseases
    • de Pablos, R.M.; Espinosa, O.; Ornedo-Hortega, R.; Cano, M.; Arguelles, S. Hydroxytyrosol protects from aging process via AMPK and autophagy; a review of its effects on cancer, metabolic syndrome, osteoporosis, immune-mediated and neurodegenerative diseases. Pharmacol. Res. 2019, 143, 58–72. [CrossRef]
    • (2019) Pharmacol. Res. , vol.143 , pp. 58-72
    • de Pablos, R.M.1    Espinosa, O.2    Ornedo-Hortega, R.3    Cano, M.4    Arguelles, S.5
  • 19
    • 54349100053 scopus 로고    scopus 로고
    • Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcohol
    • Bernini, R.; Mincione, E.; Barontini, M.; Crisante, F. Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcohol. J. Agric. Food Chem. 2008, 56, 8897–8904. [CrossRef] [PubMed]
    • (2008) J. Agric. Food Chem. , vol.56 , pp. 8897-8904
    • Bernini, R.1    Mincione, E.2    Barontini, M.3    Crisante, F.4
  • 20
    • 59049106027 scopus 로고    scopus 로고
    • A novel use of the recyclable polymer-supported IBX: An efficient chemoselective and regioselective oxidation of phenolic compounds. The case of hydroxytyrosol derivatives
    • Bernini, R.; Mincione, E.; Crisante, F.; Barontini, M.; Fabrizi, G. A novel use of the recyclable polymer-supported IBX: an efficient chemoselective and regioselective oxidation of phenolic compounds. The case of hydroxytyrosol derivatives. Tetrahedron Lett. 2009, 50, 1307–1310. [CrossRef]
    • (2009) Tetrahedron Lett , vol.50 , pp. 1307-1310
    • Bernini, R.1    Mincione, E.2    Crisante, F.3    Barontini, M.4    Fabrizi, G.5
  • 21
    • 54049146992 scopus 로고    scopus 로고
    • 2-Arylhydroxytyrosol derivatives via Suzuki-Miyaura cross-coupling
    • Bernini, R.; Cacchi, S.; Fabrizi, G.; Filisti, E. 2-Arylhydroxytyrosol derivatives via Suzuki-Miyaura cross-coupling. Org. Lett. 2008, 10, 3457–3460. [CrossRef]
    • (2008) Org. Lett. , vol.10 , pp. 3457-3460
    • Bernini, R.1    Cacchi, S.2    Fabrizi, G.3    Filisti, E.4
  • 22
    • 78650516195 scopus 로고    scopus 로고
    • Synthesis of a novel ester of hydroxytyrosol and alpha-lipoic acid exhibiting an antiproliferative effect on human colon cancer HT-29 cells
    • Bernini, R.; Crisante, F.; Merendino, N.; Molinari, R.; Soldatelli, M.C.; Velotti, F. Synthesis of a novel ester of hydroxytyrosol and alpha-lipoic acid exhibiting an antiproliferative effect on human colon cancer HT-29 cells. Eur. J. Med. Chem. 2011, 46, 439–446. [CrossRef]
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 439-446
    • Bernini, R.1    Crisante, F.2    Merendino, N.3    Molinari, R.4    Soldatelli, M.C.5    Velotti, F.6
  • 23
    • 84860306951 scopus 로고    scopus 로고
    • Convenient synthesis of 1-aryl-dihydroxyisochromans exhibiting antioxidant activity
    • Bernini, R.; Crisante, F.; Fabrizi, G.; Gentili, P. Convenient synthesis of 1-aryl-dihydroxyisochromans exhibiting antioxidant activity. Curr. Org. Chem. 2012, 16, 1051–1057. [CrossRef]
    • (2012) Curr. Org. Chem. , vol.16 , pp. 1051-1057
    • Bernini, R.1    Crisante, F.2    Fabrizi, G.3    Gentili, P.4
  • 24
    • 84977939770 scopus 로고    scopus 로고
    • Effect of hydroxytyrosol methyl carbonate on the thermal, migration and antioxidant properties of PVA based films for active food packaging
    • Fortunati, E.; Luzi, F.; Dugo, L.; Fanali, C.; Tripodo, G.; Santi, L.; Kenny, J.M.; Torre, L.; Bernini, R. Effect of hydroxytyrosol methyl carbonate on the thermal, migration and antioxidant properties of PVA based films for active food packaging. Polym. Int. 2016, 65, 872–882. [CrossRef]
    • (2016) Polym. Int. , vol.65 , pp. 872-882
    • Fortunati, E.1    Luzi, F.2    Dugo, L.3    Fanali, C.4    Tripodo, G.5    Santi, L.6    Kenny, J.M.7    Torre, L.8    Bernini, R.9
  • 26
  • 28
    • 84927126869 scopus 로고    scopus 로고
    • Ecofriendly synthesis of halogenated flavonoids and evaluation of their antifungal activity
    • Bernini, R.; Pasqualetti, M.; Provenzano, G.; Tempesta, S. Ecofriendly synthesis of halogenated flavonoids and evaluation of their antifungal activity. New J. Chem. 2015, 39, 2980–2987. [CrossRef]
    • (2015) New J. Chem. , vol.39 , pp. 2980-2987
    • Bernini, R.1    Pasqualetti, M.2    Provenzano, G.3    Tempesta, S.4
  • 29
    • 85041011468 scopus 로고    scopus 로고
    • Synthesis and evaluation of the antioxidant activity of lipophilic phenethyl trifluoroacetate esters by in vitro ABTS, DPPH and in cell-culture DCF assays
    • Bernini, R.; Barontini, M.; Cis, V.; Carastro, I.; Tofani, D.; Chiodo, R.A.; Lupattelli, P.; Incerpi, S. Synthesis and evaluation of the antioxidant activity of lipophilic phenethyl trifluoroacetate esters by in vitro ABTS, DPPH and in cell-culture DCF assays. Molecules 2018, 23, 208. [CrossRef]
    • (2018) Molecules , vol.23 , pp. 208
    • Bernini, R.1    Barontini, M.2    Cis, V.3    Carastro, I.4    Tofani, D.5    Chiodo, R.A.6    Lupattelli, P.7    Incerpi, S.8
  • 30
    • 21844433239 scopus 로고    scopus 로고
    • Efficient lipase-catalyzed synthesis of new lipid antioxidants based on a catechol structure
    • Torres de Pinedo, A.; Penalver, P.; Rondon, D.; Morales, J.C. Efficient lipase-catalyzed synthesis of new lipid antioxidants based on a catechol structure. Tetrahedron 2005, 61, 7654–7660. [CrossRef]
    • (2005) Tetrahedron , vol.61 , pp. 7654-7660
    • Torres de Pinedo, A.1    Penalver, P.2    Rondon, D.3    Morales, J.C.4
  • 32
    • 57849142518 scopus 로고    scopus 로고
    • New lipophilic tyrosyl esters. Comparative antioxidant evaluation with hydroxytyrosyl esters
    • Mateos, R.; Trujillo, M.; Pereira-Caro, G.; Madrona, A.; Cert, A.; Espartero, J. New lipophilic tyrosyl esters. Comparative antioxidant evaluation with hydroxytyrosyl esters. J. Agric. Food Chem. 2008, 56, 10960–10966. [CrossRef]
    • (2008) J. Agric. Food Chem. , vol.56 , pp. 10960-10966
    • Mateos, R.1    Trujillo, M.2    Pereira-Caro, G.3    Madrona, A.4    Cert, A.5    Espartero, J.6
  • 33
    • 77954548662 scopus 로고    scopus 로고
    • Surface-active properties of lipophilic antioxidants tyrosol and hydroxytyrosol fatty acid esters: A potential explanation for the nonlinear hypothesis of the antioxidant activity in oil-in-water emulsions
    • Lucas, R.; Comelles, F.; Alcántara, D.; Maldonado, O.S.; Curcuroze, M.; Parra, J.L.; Morales, J.C. Surface-active properties of lipophilic antioxidants tyrosol and hydroxytyrosol fatty acid esters: a potential explanation for the nonlinear hypothesis of the antioxidant activity in oil-in-water emulsions. J. Agric. Food Chem. 2010, 58, 8021–8026. [CrossRef]
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 8021-8026
    • Lucas, R.1    Comelles, F.2    Alcántara, D.3    Maldonado, O.S.4    Curcuroze, M.5    Parra, J.L.6    Morales, J.C.7
  • 34
    • 77952152454 scopus 로고    scopus 로고
    • Fatty acid hydroxytyrosyl esters: Structure/antioxidant activity relationship by ABTS and in cell-culture DCF assays
    • Tofani, D.; Balducci, V.; Gasperi, T.; Incerpi, S.; Gambacorta, A. Fatty acid hydroxytyrosyl esters: structure/antioxidant activity relationship by ABTS and in cell-culture DCF assays. J. Agric. Food Chem. 2010, 58, 5292–5299. [CrossRef]
    • (2010) J. Agric. Food Chem. , vol.58 , pp. 5292-5299
    • Tofani, D.1    Balducci, V.2    Gasperi, T.3    Incerpi, S.4    Gambacorta, A.5
  • 35
    • 84856019617 scopus 로고    scopus 로고
    • Synthesis of lipophilic tyrosyl esters derivatives and assessment of their antimicrobial and antileishmanial activities
    • Aissa, I.; Sghair, R.M.; Bouaziz, M.; Laouini, D.; Sayadi, S. Synthesis of lipophilic tyrosyl esters derivatives and assessment of their antimicrobial and antileishmanial activities. Lip. Health Dis. 2012, 11, 1–8. [CrossRef]
    • (2012) Lip. Health Dis. , vol.11 , pp. 1-8
    • Aissa, I.1    Sghair, R.M.2    Bouaziz, M.3    Laouini, D.4    Sayadi, S.5
  • 36
    • 84864751423 scopus 로고    scopus 로고
    • Synthesis and structure/antioxidant activity relationship of novel catecholic antioxidant structural analogues to hydroxytyrosol and its lipophilic esters
    • Bernini, R.; Crisante, F.; Barontini, M.; Tofani, D.; Balducci, V.; Gambacorta, A. Synthesis and structure/antioxidant activity relationship of novel catecholic antioxidant structural analogues to hydroxytyrosol and its lipophilic esters. J. Agric. Food Chem. 2012, 60, 7408–7416. [CrossRef]
    • (2012) J. Agric. Food Chem. , vol.60 , pp. 7408-7416
    • Bernini, R.1    Crisante, F.2    Barontini, M.3    Tofani, D.4    Balducci, V.5    Gambacorta, A.6
  • 37
    • 84959556624 scopus 로고    scopus 로고
    • Enzymatic synthesis of tyrosol-based phenolipids: Characterization and effect of alkyl chain unsaturation on the antioxidant activities in bulk oil and oil-in-water emulsion
    • Pande, G.; Akoh, C. Enzymatic synthesis of tyrosol-based phenolipids: characterization and effect of alkyl chain unsaturation on the antioxidant activities in bulk oil and oil-in-water emulsion. J. Am. Oil. Chem. Soc. 2016, 93, 329–337. [CrossRef]
    • (2016) J. Am. Oil. Chem. Soc. , vol.93 , pp. 329-337
    • Pande, G.1    Akoh, C.2
  • 38
    • 85037642112 scopus 로고    scopus 로고
    • Antioxidant properties of tyrosol and hydroxytyrosol saturated fatty acid
    • Sun, Y.; Zhou, D.; Shahidi, F. Antioxidant properties of tyrosol and hydroxytyrosol saturated fatty acid. Food Chem. 2018, 245, 1262–1268. [CrossRef]
    • (2018) Food Chem , vol.245 , pp. 1262-1268
    • Sun, Y.1    Zhou, D.2    Shahidi, F.3
  • 39
    • 85026197387 scopus 로고    scopus 로고
    • Preparation and antioxidant activity of tyrosoland hydroxytyrosol esters
    • Zhou, D.Y.; Sun, Y.X.; Shahidi, F. Preparation and antioxidant activity of tyrosoland hydroxytyrosol esters. J. Funct. Foods 2017, 37, 66–73. [CrossRef]
    • (2017) J. Funct. Foods , vol.37 , pp. 66-73
    • Zhou, D.Y.1    Sun, Y.X.2    Shahidi, F.3
  • 41
    • 79955039605 scopus 로고    scopus 로고
    • Revisiting the polar paradox theory: A critical overview
    • Shahidi, F.; Zhong, Y. Revisiting the polar paradox theory: A critical overview. J. Agric. Food Chem. 2011, 59, 3499–3504. [CrossRef]
    • (2011) J. Agric. Food Chem. , vol.59 , pp. 3499-3504
    • Shahidi, F.1    Zhong, Y.2
  • 42
    • 85041130320 scopus 로고    scopus 로고
    • Lipase-produced hydroxytyrosyl eicosapentaenoate is an excellent antioxidant for the stabilization of omega-3 bulk oils, emulsions and microcapsules
    • Akanbi, T.O.; Barrow, C.J. Lipase-produced hydroxytyrosyl eicosapentaenoate is an excellent antioxidant for the stabilization of omega-3 bulk oils, emulsions and microcapsules. Molecules 2018, 23, 275. [CrossRef]
    • (2018) Molecules , vol.23 , pp. 275
    • Akanbi, T.O.1    Barrow, C.J.2
  • 44
    • 82355187634 scopus 로고    scopus 로고
    • Lipophilic hydroxytyrosol esters: Fatty acid conjugates for potential topical administration
    • Procopio, A.; Celia, C.; Nardi, M.; Oliverio, M.; Paolino, D.; Sindona, G. Lipophilic hydroxytyrosol esters: fatty acid conjugates for potential topical administration. J. Nat. Prod. 2011, 74, 2377–2381. [CrossRef]
    • (2011) J. Nat. Prod. , vol.74 , pp. 2377-2381
    • Procopio, A.1    Celia, C.2    Nardi, M.3    Oliverio, M.4    Paolino, D.5    Sindona, G.6
  • 45
    • 85068535101 scopus 로고    scopus 로고
    • Process for producing concentrated and refined actives from tissues and byproducts of Olea europaea with membrane technologies
    • 2338500 A1
    • Pizzichini, D.; Russo, C.; Vitagliano, M.; Pizzichini, M.; Romani, A.; Ieri, F.; Pinelli, P.; Vignolini, P. Process for producing concentrated and refined actives from tissues and byproducts of Olea europaea with membrane technologies. Eur. Pat. Appl. 2338500 A1, 2011.
    • (2011) Eur. Pat. Appl
    • Pizzichini, D.1    Russo, C.2    Vitagliano, M.3    Pizzichini, M.4    Romani, A.5    Ieri, F.6    Pinelli, P.7    Vignolini, P.8
  • 47
    • 34548324457 scopus 로고    scopus 로고
    • Chemoselective and efficient carboxymethylation of the alcoholic chain of phenols by dimethyl carbonate (DMC)
    • Bernini, R.; Mincione, E.; Crisante, F.; Barontini, M.; Fabrizi, G.; Gentili, P. Chemoselective and efficient carboxymethylation of the alcoholic chain of phenols by dimethyl carbonate (DMC). Tetrahedron Lett. 2007, 48, 7000–7003. [CrossRef]
    • (2007) Tetrahedron Lett , vol.48 , pp. 7000-7003
    • Bernini, R.1    Mincione, E.2    Crisante, F.3    Barontini, M.4    Fabrizi, G.5    Gentili, P.6
  • 48
    • 0034843004 scopus 로고    scopus 로고
    • Antioxidant activity of hydroxytyrosol acetate compared with other olive oil polyphenols
    • Gordon, M.H.; Paiva-Martins, F.; Almeida, M. Antioxidant activity of hydroxytyrosol acetate compared with other olive oil polyphenols. J. Agric. Food Chem. 2001, 49, 2480–2485. [CrossRef]
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 2480-2485
    • Gordon, M.H.1    Paiva-Martins, F.2    Almeida, M.3
  • 49
    • 85058149889 scopus 로고    scopus 로고
    • Indentification of hydroxytyrosyl oleate, a derivative of hydroxytyrosol with anti-inflammatory properties, in olive oil by-products
    • Plastina, P.; Benincasa, C.; Perri, E.; Fazio, A.; Augimeri, G.; Poland, M.; Witkamp, R.; Meijerink, J. Indentification of hydroxytyrosyl oleate, a derivative of hydroxytyrosol with anti-inflammatory properties, in olive oil by-products. Food Chem. 2019, 279, 105–113. [CrossRef]
    • (2019) Food Chem , vol.279 , pp. 105-113
    • Plastina, P.1    Benincasa, C.2    Perri, E.3    Fazio, A.4    Augimeri, G.5    Poland, M.6    Witkamp, R.7    Meijerink, J.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.