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Volumn 63, Issue 12, 2011, Pages 780-791

Erratum: Synthesis of soluble N-functionalized polysaccharide derivatives using phenyl carbonate precursor and their application as catalysts (Starch (2011) 63: 12 DOI: 10.1002/star.201100064);Synthesis of soluble N-functionalized polysaccharide derivatives using phenyl carbonate precursor and their application as catalysts

Author keywords

Cellulose; Knoevenagel condensation; N Functionalized polysaccharides; Polysaccharide phenyl carbonate; Starch

Indexed keywords

CATALYSTS; CELLULOSE; POLYSACCHARIDES; STARCH;

EID: 82955240795     PISSN: 00389056     EISSN: 1521379X     Source Type: Journal    
DOI: 10.1002/star.201190055     Document Type: Erratum
Times cited : (18)

References (39)
  • 1
    • 0000861328 scopus 로고    scopus 로고
    • Starch modification: Challenges and prospects
    • BeMiller, J. N., Starch modification: Challenges and prospects, Starch/Stärke 1997, 49, 127-131.
    • (1997) Starch/Stärke , vol.49 , pp. 127-131
    • Bemiller, J.N.1
  • 2
  • 3
    • 67649966245 scopus 로고    scopus 로고
    • Hot topics in polysaccharide chemistry-selected examples
    • Heinze, T., Hot topics in polysaccharide chemistry-selected examples. Macromol. Symp. 2009, 280, 15-27.
    • (2009) Macromol. Symp. , vol.280 , pp. 15-27
    • Heinze, T.1
  • 7
    • 77949566695 scopus 로고    scopus 로고
    • Synthetic polymers with quaternary nitrogen atoms-Synthesis and structure of the most used type of cationic polyelectrolytes
    • Jaeger, W., Bohrisch, J., Laschewsky, A., Synthetic polymers with quaternary nitrogen atoms-Synthesis and structure of the most used type of cationic polyelectrolytes. Prog. Polym. Sci. 2010, 35, 511-577.
    • (2010) Prog. Polym. Sci. , vol.35 , pp. 511-577
    • Jaeger, W.1    Bohrisch, J.2    Laschewsky, A.3
  • 10
    • 0346752402 scopus 로고    scopus 로고
    • Film-forming aminocellulose derivatives as enzyme-compatible support matrices for biosensor developments
    • DOI 10.1023/A:1027342027945
    • Berlin, P., Klemm, D., Jung, A., Liebegott, H., Rieseler, R., Tiller, J., Film-forming aminocellulose derivatives as enzyme-compatible support matrices for biosensor developments. Cellulose 2003, 10, 343-367. (Pubitemid 37538296)
    • (2003) Cellulose , vol.10 , Issue.4 , pp. 343-367
    • Berlin, P.1    Klemm, D.2    Jung, A.3    Liebegott, H.4    Rieseler, R.5    Tiller, J.6
  • 11
    • 2542428346 scopus 로고    scopus 로고
    • Use of cationic starch derivatives for the removal of anionic dyes from textile effluents
    • DOI 10.1002/app.20386
    • Khalil, M. I., Aly, A. A., Use of cationic starch derivatives for the removal of anionic dyes from textile effluents. J. Appl. Polym. Sci. 2004, 93, 227-234. (Pubitemid 38677547)
    • (2004) Journal of Applied Polymer Science , vol.93 , Issue.1 , pp. 227-234
    • Khalil, M.I.1    Aly, A.A.2
  • 12
    • 0035442702 scopus 로고    scopus 로고
    • A review of starches and their derivatives for oilfield applications in China
    • DOI 10.1002/1521-379X(200109)53:9<401::AID-STAR401>3.0.CO;2-2
    • Zhang, L.-M., A review of starches and their derivatives for oilfield applications in China. Starch/Stärke 2001, 53, 401-407. (Pubitemid 32944546)
    • (2001) Starch/Staerke , vol.53 , Issue.9 , pp. 401-407
    • Zhang, L.-M.1
  • 13
    • 34247576699 scopus 로고    scopus 로고
    • Organic polyelectrolytes in water treatment
    • DOI 10.1016/j.watres.2007.03.012, PII S0043135407001881
    • Bolto, B., Gregory, J., Organic polyelectrolytes in water treatment. Water Res. 2007, 41, 2301-2324. (Pubitemid 46670208)
    • (2007) Water Research , vol.41 , Issue.11 , pp. 2301-2324
    • Bolto, B.1    Gregory, J.2
  • 14
    • 0029960189 scopus 로고    scopus 로고
    • Shampoos
    • DOI 10.1016/0738-081X(95)00118-Y
    • Bouillon, C., Shampoos, Clin. Dermatol. 1996, 14, 113-121. (Pubitemid 26096038)
    • (1996) Clinics in Dermatology , vol.14 , Issue.1 , pp. 113-121
    • Bouillon, C.1
  • 15
    • 0004389718 scopus 로고    scopus 로고
    • High loading cellulose based poly(alkenyl) resins for resin capture applications in halogenation reactions
    • Chesney, A., Steel, P. G., Stonehouse, D. F., High loading cellulose based poly(alkenyl) resins for resin capture applications in halogenation reactions. J. Comb. Chem. 2000, 2, 434-437.
    • (2000) J. Comb. Chem. , vol.2 , pp. 434-437
    • Chesney, A.1    Steel, P.G.2    Stonehouse, D.F.3
  • 16
    • 0034874242 scopus 로고    scopus 로고
    • Intestinal absorption of octreotide using trimethyl chitosan chloride: Studies in pigs
    • DOI 10.1023/A:1011092613951
    • Thanou, M., Verhoef, J. C., Verheijden, J. H. M., Junginger, H. E., Intestinal absorption of octreotide using trimethyl chitosan chloride: Studies in pigs. Pharm. Res. 2001, 18, 823-828. (Pubitemid 32783519)
    • (2001) Pharmaceutical Research , vol.18 , Issue.6 , pp. 823-828
    • Thanou, M.1    Verhoef, J.C.2    Verheijden, J.H.M.3    Junginger, H.E.4
  • 17
    • 0036657484 scopus 로고    scopus 로고
    • Trimethyl chitosan chloride (TMC) as a novel excipient for oral and nasal immunisation against diphtheria
    • van der Lubben, I. M., Verhoef, J. C., Fretz, M. M., van Opdorf, F. A. C., et al., Trimethyl chitosan chloride (TMC) as a novel excipient for oral and nasal immunisation against diphtheria, S.T.P. Pharma. Sci. 2002, 12, 235-242.
    • (2002) S.T.P. Pharma. Sci. , vol.12 , pp. 235-242
    • Van Der Lubben, I.M.1    Verhoef, J.C.2    Fretz, M.M.3    Van Opdorf, F.A.C.4
  • 18
    • 16344377289 scopus 로고    scopus 로고
    • Trimethylated chitosans as non-viral gene delivery vectors: Cytotoxicity and transfection efficiency
    • DOI 10.1016/j.jconrel.2005.01.001
    • Kean, T., Roth, S., Thanou, M., Trimethylated chitosans as non-viral gene delivery vectors: Cytotoxicity and transfection efficiency, J. Controlled Release 2005, 103, 643-653. (Pubitemid 40471022)
    • (2005) Journal of Controlled Release , vol.103 , Issue.3 , pp. 643-653
    • Kean, T.1    Roth, S.2    Thanou, M.3
  • 19
    • 82955209697 scopus 로고    scopus 로고
    • Ph. D. Thesis, Louisiana State University and A & M College, Baton Rouge, LA
    • Thatte, M. R., Ph. D. Thesis, Louisiana State University and A & M College, Baton Rouge, LA 2004.
    • (2004)
    • Thatte, M.R.1
  • 20
    • 0009935290 scopus 로고    scopus 로고
    • Novel Regioselectively 6-Functionalized Cationic Cellulose Polyelectrolytes Prepared via Cellulose Sulfonates
    • Koschella, A., Heinze, T., Novel regioselectively 6-functinalized cationic cellulose polyelectrolytes prepared via cellulose sulfonates, Macromol. Biosci. 2001, 1, 178-184. (Pubitemid 33641085)
    • (2001) Macromolecular Bioscience , vol.1 , Issue.5 , pp. 178-184
    • Koschella, A.1    Heinze, T.2
  • 21
    • 31544474009 scopus 로고    scopus 로고
    • Synthesis and characterization of a trifunctional aminoamide cellulose derivative
    • DOI 10.1021/bm050465n
    • Zhang, C., Price, L. M., Daly, W. H., Synthesis and characterization of a trifunctional aminoamide cellulose derivative, Biomacromolecules 2006, 7, 139-145. (Pubitemid 43154488)
    • (2006) Biomacromolecules , vol.7 , Issue.1 , pp. 139-145
    • Zhang, C.1    Price, L.M.2    Daly, W.H.3
  • 22
    • 67649960111 scopus 로고    scopus 로고
    • Unconventional cellulose products through nucleophilic displacement reactions
    • Petzold-Welcke, K., Michaelis, N., Heinze, T., Unconventional cellulose products through nucleophilic displacement reactions, Macromol. Symp. 2009, 280, 72-85.
    • (2009) Macromol. Symp. , vol.280 , pp. 72-85
    • Petzold-Welcke, K.1    Michaelis, N.2    Heinze, T.3
  • 23
    • 1642570231 scopus 로고    scopus 로고
    • Novel xylylene diaminocellulose derivatives for enzyme immobilization
    • DOI 10.1023/B:CELL.0000014763.82426.70
    • Becher, J., Liebegott, H., Berlin, P., Klemm, D., Novel xylylene diaminocellulose derivatives for enzyme immobilization, Cellulose 2004, 11, 119-126. (Pubitemid 38403510)
    • (2004) Cellulose , vol.11 , Issue.1 , pp. 119-126
    • Becher, J.1    Liebegott, H.2    Berlin, P.3    Klemm, D.4
  • 24
    • 0033896144 scopus 로고    scopus 로고
    • Novel matrices for biosensor applications by structural design of redox-chromogenic aminocellulose esters
    • DOI 10.1002/(SICI)1097-4628(20000214)75:7<904::AID-APP7>3.0.CO;2-8
    • Tiller, J., Berlin, P., Klemm, D., Novel matrices for biosensor applications by structural design of redox-chromogenic aminocellulose esters, J. Appl. Polym. Sci. 2000, 75, 904-915. (Pubitemid 30527132)
    • (2000) Journal of Applied Polymer Science , vol.75 , Issue.7 , pp. 904-915
    • Tiller, J.1    Berlin, P.2    Klemm, D.3
  • 25
    • 33747828097 scopus 로고
    • Preparation and synthetic application of cellulose-supported phase transfer catalysts
    • Akelah, A., Sherrington, D. C., Preparation and synthetic application of cellulose-supported phase transfer catalysts, Eur. Polym. J. 1982, 18, 301-305.
    • (1982) Eur. Polym. J. , vol.18 , pp. 301-305
    • Akelah, A.1    Sherrington, D.C.2
  • 26
    • 0002512542 scopus 로고    scopus 로고
    • Soluble and film-forming cellulose derivatives with redox-chromogenic and enzyme immobilizing 1,4-phenylenediamine groups
    • Tiller, J., Berlin, P., Klemm, D., Soluble and film-forming cellulose derivatives with redox-chromogenic and enzyme immobilizing 1,4-phenylenediamine groups, Macromol. Chem. Phys. 1999, 200, 1-9. (Pubitemid 129696078)
    • (1999) Macromolecular Chemistry and Physics , vol.200 , Issue.1 , pp. 1-9
    • Tiller, J.1    Berlin, P.2    Klemm, D.3
  • 27
    • 0037118930 scopus 로고    scopus 로고
    • Exclusive and complete introduction of amino groups and their N-sulfo and N-carboxymethyl groups into the 6-position of cellulose without the use of protecting groups
    • DOI 10.1016/S0008-6215(02)00132-5, PII S0008621502001325
    • Liu, C., Baumann, H., Exclusive and complete introduction of amino groups and their N-sulfo and N-carboxymethyl groups into the 6-position of cellulose without the use of protecting groups, Carbohydr. Res. 2002, 337, 1297-1307. (Pubitemid 34874760)
    • (2002) Carbohydrate Research , vol.337 , Issue.14 , pp. 1297-1307
    • Liu, C.1    Baumann, H.2
  • 28
    • 55349126072 scopus 로고    scopus 로고
    • Novel biopolymer structures synthesized by dendronization of 6-deoxy-6-aminopropargyl cellulose
    • Pohl, M., Heinze, T., Novel biopolymer structures synthesized by dendronization of 6-deoxy-6-aminopropargyl cellulose, Macromol. Rapid Commun. 2008, 29, 1739-1745.
    • (2008) Macromol. Rapid Commun. , vol.29 , pp. 1739-1745
    • Pohl, M.1    Heinze, T.2
  • 29
    • 3242688626 scopus 로고    scopus 로고
    • Starch derivatives of high degree of functionalization. 7. Preparation of cationic 2-hydroxypropyltrimethylammonium chloride starches
    • Heinze, T., Haack, V., Rensing, S., Starch derivatives of high degree of functionalization. 7. Preparation of cationic 2-hydroxypropyltrimethylammonium chloride starches, Starch/Stärke 2004, 56, 288-296.
    • (2004) Starch/Stärke , vol.56 , pp. 288-296
    • Heinze, T.1    Haack, V.2    Rensing, S.3
  • 31
    • 0036128916 scopus 로고    scopus 로고
    • Synthesis and properties of cellulose carbonate derivatives
    • Hayashi, S., Synthesis and properties of cellulose carbonate derivatives. Kobunshi Ronbunshu (Japanese J. Polym. Sci. Technol.) 2002, 59, 1-7. (Pubitemid 34235585)
    • (2002) Kobunshi Ronbunshu , vol.59 , Issue.1 , pp. 1-7
    • Hayashi, S.1
  • 33
    • 0035804384 scopus 로고    scopus 로고
    • Functionalized polymers - Emerging versatile tools for solution-phase chemistry and automated parallel synthesis
    • DOI 10.1002/1521-3773(20010216)40:4<650::AID-ANIE6500>3.0.CO;2-C
    • Kirschning, A., Monenschein, H., Wittenberg, R., Functionalized polymers-emerging versatile tools for solution-phase chemistry and automated parallel synthesis. Angew. Chem., Int. Ed. 2001, 40, 650-679. (Pubitemid 32179720)
    • (2001) Angewandte Chemie - International Edition , vol.40 , Issue.4 , pp. 650-679
    • Kirschning, A.1    Monenschein, H.2    Wittenberg, R.3
  • 34
    • 20844433475 scopus 로고    scopus 로고
    • Multi-step organic synthesis using solid-supported reagents and scavengers: A new paradigm in chemical library generation
    • Ley, S. V., Baxendale, I. R., Bream, R. N., Jackson, P. S., et al., Multi-step organic synthesis using solid-supported reagents and scavengers: a new paradigm in chemical library generation, J. Chem. Soc., Perkin Trans. 1, 2000, 23, 3815-4195.
    • (2000) J. Chem. Soc., Perkin Trans. 1 , vol.23 , pp. 3815-4195
    • Ley, S.V.1    Baxendale, I.R.2    Bream, R.N.3    Jackson, P.S.4
  • 35
    • 34247234108 scopus 로고    scopus 로고
    • Applications of polymeric reagents in organic synthesis
    • Salimi, H., Rahimi, A., Pourjavadi, A., Applications of polymeric reagents in organic synthesis, Monatshefte für Chemie 2007, 138, 363-379.
    • (2007) Monatshefte für Chemie , vol.138 , pp. 363-379
    • Salimi, H.1    Rahimi, A.2    Pourjavadi, A.3
  • 36
    • 0036811238 scopus 로고    scopus 로고
    • Soluble polymers as scaffolds for recoverable catalysts and reagents
    • DOI 10.1021/cr010335e
    • Dickerson, T. J., Reed, N. N., Janda, K. D., Soluble polymers as scaffolds for recoverable catalysts and reagents, Chem. Rev. 2002, 102, 3325-3344. (Pubitemid 35350654)
    • (2002) Chemical Reviews , vol.102 , Issue.10 , pp. 3325-3344
    • Dickerson, T.J.1    Reed, N.N.2    Janda, K.D.3
  • 38
    • 0006371019 scopus 로고
    • Studies on geometric isomerism by nuclear magnetic resonance. III. Stereochemistry of α-cyanocinnamic esters
    • Hayashi, T., Studies on geometric isomerism by nuclear magnetic resonance. III. Stereochemistry of α-cyanocinnamic esters, J. Org. Chem. 1966, 31, 3253.
    • (1966) J. Org. Chem. , vol.31 , pp. 3253
    • Hayashi, T.1
  • 39
    • 33845184170 scopus 로고
    • Ruthenium-catalyzed aldol and Michael reactions of activated nitriles
    • Naota, T., Taki, H., Mizuno, M., Murahashi, S.-I., Ruthenium-catalyzed aldol and Michael reactions of activated nitriles, J. Am. Chem. Soc. 1989, 111, 5954-5955.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 5954-5955
    • Naota, T.1    Taki, H.2    Mizuno, M.3    Murahashi, S.-I.4


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