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Volumn 48, Issue 5, 1996, Pages 191-195

Synthesis of cyanoethyl inulin, aminopropyl inulin and carboxyethyl inulin

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EID: 0002913829     PISSN: 00389056     EISSN: None     Source Type: Journal    
DOI: 10.1002/star.19960480509     Document Type: Article
Times cited : (22)

References (18)
  • 1
    • 0021577493 scopus 로고
    • Mechanical Properties of Paper Sheets Prepared from Partially Cyanoethylated Wood Pulp
    • El-Shinnawy, N. A., and S. F. El-Kalyoubi: Mechanical Properties of Paper Sheets Prepared from Partially Cyanoethylated Wood Pulp. J. Appl. Pol. Sci. 29 (1984), 4329-4333.
    • (1984) J. Appl. Pol. Sci. , vol.29 , pp. 4329-4333
    • El-Shinnawy, N.A.1    El-Kalyoubi, S.F.2
  • 2
    • 85033006861 scopus 로고
    • U. S. Pat. 2535690 General Electric Co.; Abstr. 45 (1951) 3533
    • Miller, H. F. and R. G. Flowers: U. S. Pat. 2535690 (1950), General Electric Co.; Abstr. 45 (1951) 3533.
    • (1950)
    • Miller, H.F.1    Flowers, R.G.2
  • 3
    • 0027311690 scopus 로고
    • Kinetics of Heterogeneous Cyanoethylation of Cellulose
    • Sefain, M. Z., M. H. Fadl, N. A. Elwakil, and M. M. Naoum: Kinetics of Heterogeneous Cyanoethylation of Cellulose. Polymer Int. 32 (1993), 251-255.
    • (1993) Polymer Int. , vol.32 , pp. 251-255
    • Sefain, M.Z.1    Fadl, M.H.2    Elwakil, N.A.3    Naoum, M.M.4
  • 4
    • 84989036208 scopus 로고
    • Characterization of the Reaction Products of Starch and Acrylonitrile
    • Hebeish, A., and M.I. Khalil: Characterization of the Reaction Products of Starch and Acrylonitrile. Starch/Stärke 40 (1988), 104-107.
    • (1988) Starch/Stärke , vol.40 , pp. 104-107
    • Hebeish, A.1    Khalil, M.I.2
  • 5
    • 84980088525 scopus 로고
    • The reaction of Acrylonitrile with Macromolecular Hydroxy Substances. I. General Survey of the Reaction
    • MacGregor, J. H.: The reaction of Acrylonitrile with Macromolecular Hydroxy Substances. I. General Survey of the Reaction. J. Soc. Dyers and Colorists 67 (1951), 66-73.
    • (1951) J. Soc. Dyers and Colorists , vol.67 , pp. 66-73
    • MacGregor, J.H.1
  • 8
    • 0004356308 scopus 로고
    • Ethers from α,β-Unsaturated Compounds
    • Eds. N. M. Bikales and L. Segal. Wiley Interscience, New York
    • Bikales, N.M.: Ethers from α,β-Unsaturated Compounds, in: Cellulose and Cellulose Derivatives, Part V. Eds. N. M. Bikales and L. Segal. Wiley Interscience, New York 1971, pp. 811-833.
    • (1971) Cellulose and Cellulose Derivatives , Issue.5 PART , pp. 811-833
    • Bikales, N.M.1
  • 9
    • 0004490085 scopus 로고
    • Kinetics and Mechanism of the Cyanoethylation of Alcohols
    • Feit, B. A., and A. Zilkha: Kinetics and Mechanism of the Cyanoethylation of Alcohols, J. Org. Chem. 28 (1963), 406-410.
    • (1963) J. Org. Chem. , vol.28 , pp. 406-410
    • Feit, B.A.1    Zilkha, A.2
  • 12
    • 0028483292 scopus 로고
    • Homogeneous and Heterogeneous Hydrogenation of Nitriles in a Liquid Phase: Chemical, Mechanistic, and Catalytic Aspects
    • De Bellefon, C., and P. Fouilloux: Homogeneous and Heterogeneous Hydrogenation of Nitriles in a Liquid Phase: Chemical, Mechanistic, and Catalytic Aspects. Rev.-Sci. Eng. 36 (1994), 459-506.
    • (1994) Rev.-Sci. Eng. , vol.36 , pp. 459-506
    • De Bellefon, C.1    Fouilloux, P.2
  • 13
    • 0002728573 scopus 로고
    • Reduction of the Cyano Group
    • Ed. Z. Rappoport. Interscience Publishers, London
    • Rabinovitz, M.: Reduction of the Cyano Group, in: The Chemistry of the Cyano Group. Ed. Z. Rappoport. Interscience Publishers, London 1970, pp. 307-340.
    • (1970) The Chemistry of the Cyano Group , pp. 307-340
    • Rabinovitz, M.1
  • 14
    • 0000271946 scopus 로고
    • Reduction of Organic Compounds with Sodium Borohydride-Transition Metal Systems. 1. Reduction of Organic Nitrile, Nitro and Amide Compounds to Primary Amines
    • Satoh, T., S. Suzuki, Y. Suzuki, Y. Miyaji, and Z. Imai: Reduction of Organic Compounds with Sodium Borohydride-Transition Metal Systems. 1. Reduction of Organic Nitrile, Nitro and Amide Compounds to Primary Amines. Tetrahedron Lett. 52 (1969), 4555-4558.
    • (1969) Tetrahedron Lett. , vol.52 , pp. 4555-4558
    • Satoh, T.1    Suzuki, S.2    Suzuki, Y.3    Miyaji, Y.4    Imai, Z.5
  • 15
    • 0002612174 scopus 로고
    • Nitrile Reactivity
    • Ed. Z. Rappoport. Interscience Publishers, London
    • Schaefer, F.C.: Nitrile Reactivity, in: The Chemistry of the Cyano Group. Ed. Z. Rappoport. Interscience Publishers, London 1970, pp. 239-305.
    • (1970) The Chemistry of the Cyano Group , pp. 239-305
    • Schaefer, F.C.1
  • 16
    • 85033002678 scopus 로고
    • Inter-and Intramolecular Reactions of Coordinated Nitriles
    • Eds. T. G. Spiro. New York
    • Dixon, N. E., and A. M. Sargeson: Inter-and Intramolecular Reactions of Coordinated Nitriles, in: Zinc Enzymes. Eds. T. G. Spiro. New York 1983, pp. 261-266.
    • (1983) Zinc Enzymes , pp. 261-266
    • Dixon, N.E.1    Sargeson, A.M.2
  • 17
    • 33847800530 scopus 로고
    • A Rapid Procedure for the Hydrolysis of Amides to Acids
    • Vaughn, H. L., and M. D. Robbins: A Rapid Procedure for the Hydrolysis of Amides to Acids. J. Org. Chem. 40 (1975), 1187-1189.
    • (1975) J. Org. Chem. , vol.40 , pp. 1187-1189
    • Vaughn, H.L.1    Robbins, M.D.2
  • 18
    • 84984191293 scopus 로고
    • Amides from Nitriles using Basic Hydrogen Peroxide under Phase-Transfer Catalyzed Conditions
    • Cacchi, S., D. Misiti, and F. La Torre: Amides from Nitriles using Basic Hydrogen Peroxide under Phase-Transfer Catalyzed Conditions. Synthesis (1980), 243-244.
    • (1980) Synthesis , pp. 243-244
    • Cacchi, S.1    Misiti, D.2    La Torre, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.