메뉴 건너뛰기




Volumn 26, Issue 3, 2001, Pages 379-441

Synthesis of polysaccharides having specific biological activities

Author keywords

Amino polysaccharides; Amino sugars; Anhydro disaccharides; Anhydro sugars; Anti HIV activity; Anti tumor activity; Blood anti coagulant activity; Branched polysaccharides; Deoxy polysaccharides; Enzymatic polymerization; Ring opening polymerization; Sulfonated polysaccharides; Wound healing activity

Indexed keywords

AMINO ACIDS; DERIVATIVES; ENZYME KINETICS; RING OPENING POLYMERIZATION; STEREOCHEMISTRY; SULFONATION; SYNTHESIS (CHEMICAL);

EID: 0035304719     PISSN: 00796700     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0079-6700(00)00045-9     Document Type: Review
Times cited : (83)

References (157)
  • 1
    • 0008522753 scopus 로고
    • Distillation of cellulose and starch in vacuo
    • Pictet A., Sarasin V. Distillation of cellulose and starch in vacuo. Helv Chim Acta. 1:1918;78-96.
    • (1918) Helv Chim Acta , vol.1 , pp. 78-96
    • Pictet, A.1    Sarasin, V.2
  • 2
    • 84977257872 scopus 로고
    • Transformation of levoglucosan into dextrin
    • Pictet A. Transformation of levoglucosan into dextrin. Helv Chim Acta. 1:1918;226-230.
    • (1918) Helv Chim Acta , vol.1 , pp. 226-230
    • Pictet, A.1
  • 3
    • 0000168867 scopus 로고
    • Preparation of high polymers from 1,6-anhydo-2,3,4-tri-O-substituted β-D-glucopyranose
    • Ruckel E.R., Schuerch C. Preparation of high polymers from 1,6-anhydo-2,3,4-tri-O-substituted β-D-glucopyranose. J Org Chem. 31:1966;2233-2238.
    • (1966) J Org Chem , vol.31 , pp. 2233-2238
    • Ruckel, E.R.1    Schuerch, C.2
  • 4
    • 0023185808 scopus 로고
    • Antiretroviral activity in a marine red alga: Reverse transcriptase inhibition by an aqueous extract of Schizymenia pacifica
    • Nakashima H., Kido Y., Kobayashi N., Motoki Y., Neushul M., Yamamoto N. Antiretroviral activity in a marine red alga: reverse transcriptase inhibition by an aqueous extract of Schizymenia pacifica. J Cancer Res Clin Oncol. 113:1987;413-416.
    • (1987) J Cancer Res Clin Oncol , vol.113 , pp. 413-416
    • Nakashima, H.1    Kido, Y.2    Kobayashi, N.3    Motoki, Y.4    Neushul, M.5    Yamamoto, N.6
  • 5
    • 0023634895 scopus 로고
    • Purification and characterization of an avian myeloblastosis and human immunodeficiency virus reverse transcriptase inhibitor, sulfated polysaccharides extracted from sea algae
    • Nakashima H., Kido Y., Kobayashi N., Motoki Y., Neushul M., Yamamoto N. Purification and characterization of an avian myeloblastosis and human immunodeficiency virus reverse transcriptase inhibitor, sulfated polysaccharides extracted from sea algae. Antimicrob Agents Chemother. 31:1987;1524-1528.
    • (1987) Antimicrob Agents Chemother , vol.31 , pp. 1524-1528
    • Nakashima, H.1    Kido, Y.2    Kobayashi, N.3    Motoki, Y.4    Neushul, M.5    Yamamoto, N.6
  • 7
    • 0038277150 scopus 로고
    • Artificial polysaccharides and their biological activities
    • Uryu T. Artificial polysaccharides and their biological activities. Prog Polym Sci. 18:1993;717-761.
    • (1993) Prog Polym Sci , vol.18 , pp. 717-761
    • Uryu, T.1
  • 9
    • 0012261562 scopus 로고
    • The chemical synthesis and properties of polysaccharides of biomediated interest
    • Schuerch C. The chemical synthesis and properties of polysaccharides of biomediated interest. Adv Polym Sci. 10:1972;173-194.
    • (1972) Adv Polym Sci , vol.10 , pp. 173-194
    • Schuerch, C.1
  • 10
    • 0000672337 scopus 로고
    • Synthesis and polymerization of anhydro sugars
    • Schuerch C. Synthesis and polymerization of anhydro sugars. Adv Polym Sci. 39:1981;157-212.
    • (1981) Adv Polym Sci , vol.39 , pp. 157-212
    • Schuerch, C.1
  • 11
    • 11944265905 scopus 로고
    • Ring-opening polymerization of bicyclic and spiro compounds. Reactivities and polymerization mechanisms
    • Okada M. Ring-opening polymerization of bicyclic and spiro compounds. Reactivities and polymerization mechanisms. Adv Polym Sci. 102:1992;1-46.
    • (1992) Adv Polym Sci , vol.102 , pp. 1-46
    • Okada, M.1
  • 12
    • 85052581130 scopus 로고    scopus 로고
    • Chemical synthesis of polysaccharides
    • S. Dumitriu. New York: Marcel Dekker
    • Hatanaka K. Chemical synthesis of polysaccharides. Dumitriu S. Polysaccharides in medical applications. 1996;3-20 Marcel Dekker, New York.
    • (1996) Polysaccharides in Medical Applications , pp. 3-20
    • Hatanaka, K.1
  • 13
    • 0001916271 scopus 로고
    • The pyrolysis of cellulose and the action of flame-retardants II. Further analysis and identification of products
    • Byrne G.A., Gardiner D., Holmes F.H. The pyrolysis of cellulose and the action of flame-retardants II. Further analysis and identification of products. J Appl Chem. 16:1966;81-88.
    • (1966) J Appl Chem , vol.16 , pp. 81-88
    • Byrne, G.A.1    Gardiner, D.2    Holmes, F.H.3
  • 14
    • 0029078472 scopus 로고
    • Microwave assisted organic reactions
    • Caddick S. Microwave assisted organic reactions. Tetrahedron. 38:1995;10,403-10,432.
    • (1995) Tetrahedron , vol.38 , pp. 10
    • Caddick, S.1
  • 15
    • 84924213784 scopus 로고
    • Developments in microwave-assisted organic chemistry
    • Strauss C.R., Trainor R.W. Developments in microwave-assisted organic chemistry. Aust J Chem. 48:1995;1665-1692.
    • (1995) Aust J Chem , vol.48 , pp. 1665-1692
    • Strauss, C.R.1    Trainor, R.W.2
  • 16
    • 0019059716 scopus 로고
    • Dielectric loss microwave degradation of polymers: Cellulose
    • Allan G.G., Krieger B.B., Work D.W. Dielectric loss microwave degradation of polymers: cellulose. J Appl Polym Sci. 25:1980;1839-1859.
    • (1980) J Appl Polym Sci , vol.25 , pp. 1839-1859
    • Allan, G.G.1    Krieger, B.B.2    Work, D.W.3
  • 17
    • 84987080876 scopus 로고
    • Preparation of 1,6-anhydro-glucose from 1,4-β-glucans using microwave technology
    • Straathof J.J., van Bekkum H., Kieboom A.P.G. Preparation of 1,6-anhydro-glucose from 1,4-β-glucans using microwave technology. Recl Trav Chim Pays-Bas. 107:1988;647-648.
    • (1988) Recl Trav Chim Pays-Bas , vol.107 , pp. 647-648
    • Straathof, J.J.1    Van Bekkum, H.2    Kieboom, A.P.G.3
  • 18
    • 0001391706 scopus 로고
    • A new microwave reactor for batchwise organic synthesis
    • Raner K.S., Strauss C.R., Trainor R.W., Trainor R.W. A new microwave reactor for batchwise organic synthesis. J Org Chem. 60:1995;2456-2460.
    • (1995) J Org Chem , vol.60 , pp. 2456-2460
    • Raner, K.S.1    Strauss, C.R.2    Trainor, R.W.3    Trainor, R.W.4
  • 20
    • 0142129332 scopus 로고    scopus 로고
    • Refinement of levoglucosan in wood pyroligneous liquor
    • Miura M., Tanaka R. Refinement of levoglucosan in wood pyroligneous liquor. Mokuzai Gakkai-shi. 42:1996;318-321.
    • (1996) Mokuzai Gakkai-shi , vol.42 , pp. 318-321
    • Miura, M.1    Tanaka, R.2
  • 21
    • 33749144091 scopus 로고
    • Experiments on the polycondensation of 2,3,6-tri-O-benzyl-D-glucopyranose and polymerization of 1,4-anhydro-β-D-glucopyranose
    • Micheel F., Brodde O., Reinking K. Experiments on the polycondensation of 2,3,6-tri-O-benzyl-D-glucopyranose and polymerization of 1,4-anhydro-β-D-glucopyranose. Justus Liebigs Ann Chem. 1974;124-136.
    • (1974) Justus Liebigs Ann Chem , pp. 124-136
    • Micheel, F.1    Brodde, O.2    Reinking, K.3
  • 22
    • 0343823478 scopus 로고
    • Synthesis of 1,4-anhydro-β-D-glucopyranose derivatives having acyl groups
    • Kamitakahara H., Nakatsubo F., Murakami K. Synthesis of 1,4-anhydro-β-D-glucopyranose derivatives having acyl groups. Mokuzai Gakkai-shi. 40:1994;302-307.
    • (1994) Mokuzai Gakkai-shi , vol.40 , pp. 302-307
    • Kamitakahara, H.1    Nakatsubo, F.2    Murakami, K.3
  • 24
    • 0343387845 scopus 로고
    • Polymerization of 1,6-anhydro-β-D-galactofuranose
    • Lin J.W., Schuerch C. Polymerization of 1,6-anhydro-β-D-galactofuranose. Macromolecules. 2:1972;656-657.
    • (1972) Macromolecules , vol.2 , pp. 656-657
    • Lin, J.W.1    Schuerch, C.2
  • 25
    • 0030021884 scopus 로고    scopus 로고
    • An improved synthesis of 1,6-anhydro-2,3-di-O-benzyl-β-D-xylo-hexopyranos-4-ulose
    • Caron S., McDonald A.I., Heathcock C.H. An improved synthesis of 1,6-anhydro-2,3-di-O-benzyl-β-D-xylo-hexopyranos-4-ulose. Carbohydr Res. 281:1996;179-182.
    • (1996) Carbohydr Res , vol.281 , pp. 179-182
    • Caron, S.1    McDonald, A.I.2    Heathcock, C.H.3
  • 26
    • 0033472865 scopus 로고    scopus 로고
    • An efficient method for the synthesis of a 1,6-anhydro-β-D-galactofuranose derivative and its application in the synthesis of oligosaccharides
    • Sarkar S.K., Choudhury A.K., Mukhopadhyay B., Roy N. An efficient method for the synthesis of a 1,6-anhydro-β-D-galactofuranose derivative and its application in the synthesis of oligosaccharides. J Carbohydr Res. 18:1999;1121-1130.
    • (1999) J Carbohydr Res , vol.18 , pp. 1121-1130
    • Sarkar, S.K.1    Choudhury, A.K.2    Mukhopadhyay, B.3    Roy, N.4
  • 27
    • 0342952375 scopus 로고    scopus 로고
    • Synthesis and polymerization of 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-talopyranose
    • 25 p.
    • Yoshida T, Tsukuda T. Synthesis and polymerization of 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-talopyranose. Abstr 75th Chem Soc Jpn, 1998. 25 p.
    • (1998) Abstr 75th Chem Soc Jpn
    • Yoshida, T.1    Tsukuda, T.2
  • 28
    • 0023964141 scopus 로고
    • Sterically controlled ring-opening polymerization of a 1,6-β-D-galactopyranose derivative by neighboring group participation: (1→6)-β-D-galactopyranan
    • Kobayashi K., Ichikawa H., Sumitomo H., Schuerch C. Sterically controlled ring-opening polymerization of a 1,6-β-D-galactopyranose derivative by neighboring group participation: (1→6)-β-D-galactopyranan. Macromolecules. 21:1988;542-543.
    • (1988) Macromolecules , vol.21 , pp. 542-543
    • Kobayashi, K.1    Ichikawa, H.2    Sumitomo, H.3    Schuerch, C.4
  • 29
    • 0005551420 scopus 로고
    • Synthesis of a β-(1→6)-linked polysaccharide via ring-opening polymerization with neighboring-group participation
    • Ichikawa H., Kobayashi K., Sumitomo H., Schuerch C. Synthesis of a β-(1→6)-linked polysaccharide via ring-opening polymerization with neighboring-group participation. Carbohydr Res. 179:1988;315-320.
    • (1988) Carbohydr Res , vol.179 , pp. 315-320
    • Ichikawa, H.1    Kobayashi, K.2    Sumitomo, H.3    Schuerch, C.4
  • 30
    • 0027289770 scopus 로고
    • Steric control in ring-opening polymerization of 1,6-anhydro-galactose derivatives by neighboring group participation
    • Kobayashi K., Ishii T., Okada M., Schuerch C. Steric control in ring-opening polymerization of 1,6-anhydro-galactose derivatives by neighboring group participation. Polym J. 25:1993;49-57.
    • (1993) Polym J , vol.25 , pp. 49-57
    • Kobayashi, K.1    Ishii, T.2    Okada, M.3    Schuerch, C.4
  • 31
    • 0343387844 scopus 로고
    • Regioselectively modified stereoregular polysaccharide. 1. Polymerization of 1,6-anhydro-3-O-acetyl-2,4-di-O-benzyl-β-D-glucopyranose and synthesis of 2,4-di-O-benzyl-(1→6)-β-D-glucopyranan
    • Kobayashi K., Sumitomo H., Yasui A. Regioselectively modified stereoregular polysaccharide. 1. Polymerization of 1,6-anhydro-3-O-acetyl-2,4-di-O-benzyl-β-D-glucopyranose and synthesis of 2,4-di-O-benzyl-(1→6)-β-D-glucopyranan. Macromolecules. 12:1979;1019-1023.
    • (1979) Macromolecules , vol.12 , pp. 1019-1023
    • Kobayashi, K.1    Sumitomo, H.2    Yasui, A.3
  • 32
    • 0042476913 scopus 로고
    • Regioselectively modified stereoregular polysaccharide. 2. Synthesis of 3-O-methyl-(1→6)-α-D-glucopyranan
    • Kobayashi K., Sumitomo H. Regioselectively modified stereoregular polysaccharide. 2. Synthesis of 3-O-methyl-(1→6)-α-D-glucopyranan. Macromolecules. 14:1981;250-253.
    • (1981) Macromolecules , vol.14 , pp. 250-253
    • Kobayashi, K.1    Sumitomo, H.2
  • 33
    • 0343387843 scopus 로고
    • Regioselectively modified stereoregular polysaccharide. 6. Synthesis of 3-deoxy-(1→6)-α-ribo-D-glucopyranan
    • Kobayashi K., Sumitomo H. Regioselectively modified stereoregular polysaccharide. 6. Synthesis of 3-deoxy-(1→6)-α-ribo-D-glucopyranan. Macromolecules. 16:1983;710-711.
    • (1983) Macromolecules , vol.16 , pp. 710-711
    • Kobayashi, K.1    Sumitomo, H.2
  • 34
    • 0025462550 scopus 로고
    • Regioselectively modified stereoregular polysaccharides. 11. Synthesis of (1→6)-α-D-glucopyranans having one long hydrocarbon chain in position 3 in each repeating unit
    • Kobayashi K., Ichikawa H., Sumitomo H. Regioselectively modified stereoregular polysaccharides. 11. Synthesis of (1→6)-α-D-glucopyranans having one long hydrocarbon chain in position 3 in each repeating unit. Macromolecules. 23:1990;3708-3710.
    • (1990) Macromolecules , vol.23 , pp. 3708-3710
    • Kobayashi, K.1    Ichikawa, H.2    Sumitomo, H.3
  • 35
    • 0031244953 scopus 로고    scopus 로고
    • Synthesis of a regioselectively fluorinated polysaccharide 3-deoxy-3-fluoro-(1→6)-α-D-glucopyranan via ring-opening polymerization
    • Kobayashi K., Tadano T. Synthesis of a regioselectively fluorinated polysaccharide 3-deoxy-3-fluoro-(1→6)-α-D-glucopyranan via ring-opening polymerization. Macromolecules. 30:1997;6531-6535.
    • (1997) Macromolecules , vol.30 , pp. 6531-6535
    • Kobayashi, K.1    Tadano, T.2
  • 36
    • 33751340062 scopus 로고
    • Selective ring-opening polymerization of 1,4-anhydro-α-D-ribopyranose derivative and synthesis of stereoregular (1→4)-β-D-ribopyranan
    • Uryu T., Kitano K., Ito K., Yamanouchi J., Matsuzaki K. Selective ring-opening polymerization of 1,4-anhydro-α-D-ribopyranose derivative and synthesis of stereoregular (1→4)-β-D-ribopyranan. Macromolecules. 14:1981;1-9.
    • (1981) Macromolecules , vol.14 , pp. 1-9
    • Uryu, T.1    Kitano, K.2    Ito, K.3    Yamanouchi, J.4    Matsuzaki, K.5
  • 37
    • 0020848782 scopus 로고
    • Selective ring-opening polymerization of di-O-methylated and di-O-benzylated 1,4-anhydro-β-D-ribopyranoses and structure proof of synthetic cellulose-type polysaccharide (1→4)-β-D-ribopyranan and (1→5)-α-D-ribofuranan
    • Uryu T., Yamanouchi J., Kato T., Higichi S., Matsuzaki K. Selective ring-opening polymerization of di-O-methylated and di-O-benzylated 1,4-anhydro-β-D-ribopyranoses and structure proof of synthetic cellulose-type polysaccharide (1→4)-β-D-ribopyranan and (1→5)-α-D-ribofuranan. J Am Chem Soc. 105:1983;6865-6871.
    • (1983) J Am Chem Soc , vol.105 , pp. 6865-6871
    • Uryu, T.1    Yamanouchi, J.2    Kato, T.3    Higichi, S.4    Matsuzaki, K.5
  • 38
    • 0342772837 scopus 로고
    • Selective ring-opening polymerization of 1,4-anhydro-2,3-di-O-benzyl-α-D-xylopyranose and synthesis of stereoregular (1→5)-α-D-xylofuranan
    • Uryu T., Yamanouchi J., Hayashi S., Tamaki H., Matsuzaki K. Selective ring-opening polymerization of 1,4-anhydro-2,3-di-O-benzyl-α-D-xylopyranose and synthesis of stereoregular (1→5)-α-D-xylofuranan. Macromolecules. 16:1983;320-326.
    • (1983) Macromolecules , vol.16 , pp. 320-326
    • Uryu, T.1    Yamanouchi, J.2    Hayashi, S.3    Tamaki, H.4    Matsuzaki, K.5
  • 39
    • 0342952372 scopus 로고
    • Selective ring-opening polymerization of 1,4-anhydro-α-D-lyxopyranose derivatives and synthesis of stereoregular (1→5)-α-D-lyxofuranan
    • Hagino A., Yoshida S., Shinpuku T., Matsuzaki K., Uryu T. Selective ring-opening polymerization of 1,4-anhydro-α-D-lyxopyranose derivatives and synthesis of stereoregular (1→5)-α-D-lyxofuranan. Macromolecules. 19:1986;1-7.
    • (1986) Macromolecules , vol.19 , pp. 1-7
    • Hagino, A.1    Yoshida, S.2    Shinpuku, T.3    Matsuzaki, K.4    Uryu, T.5
  • 40
    • 0022212668 scopus 로고
    • Catiojic ring-opening polymerization of 1,4-anhydro-2,3-di-O-benzyl-α-L-arabinopyranose and synthesis of L-arabinofuranan
    • Koyama Y., Harima K., Matsuzaki K., Uryu T. Catiojic ring-opening polymerization of 1,4-anhydro-2,3-di-O-benzyl-α-L-arabinopyranose and synthesis of L-arabinofuranan. J Polym Sci Polym Chem Ed. 23:1985;2989-2998.
    • (1985) J Polym Sci Polym Chem Ed , vol.23 , pp. 2989-2998
    • Koyama, Y.1    Harima, K.2    Matsuzaki, K.3    Uryu, T.4
  • 41
    • 0024047828 scopus 로고
    • Selective synthesis of polysaccharide macromonomers by ring-opening polymerization of anhydro sugar
    • Uryu T., Yamanaka M., Date M., Ogawa M., Hatanaka K. Selective synthesis of polysaccharide macromonomers by ring-opening polymerization of anhydro sugar. Macromolecules. 21:1988;1916-1920.
    • (1988) Macromolecules , vol.21 , pp. 1916-1920
    • Uryu, T.1    Yamanaka, M.2    Date, M.3    Ogawa, M.4    Hatanaka, K.5
  • 42
    • 0023591604 scopus 로고
    • Selective ring-opening polymerization of di-O-tert-butyldimethylsilylated and di-O-p-bromobenzylated 1,4-anhydro-α-L-arabinopyranoses and structural analysis of free arabinans
    • Yoshida T., Kida M., Uryu T. Selective ring-opening polymerization of di-O-tert-butyldimethylsilylated and di-O-p-bromobenzylated 1,4-anhydro-α-L-arabinopyranoses and structural analysis of free arabinans. Polym J. 19:1987;923-931.
    • (1987) Polym J , vol.19 , pp. 923-931
    • Yoshida, T.1    Kida, M.2    Uryu, T.3
  • 43
    • 0024287885 scopus 로고
    • Synthesis of branched D-xylofuranan by selective ring-opening polymerization of silylated 1,5-anhydro-β-D-xylopyranose and its conversion into a blood anticoagulant
    • Yoshida T., Arai T., Mukai Y., Uryu T. Synthesis of branched D-xylofuranan by selective ring-opening polymerization of silylated 1,5-anhydro-β-D-xylopyranose and its conversion into a blood anticoagulant. Carbohydr Res. 177:1988;69-80.
    • (1988) Carbohydr Res , vol.177 , pp. 69-80
    • Yoshida, T.1    Arai, T.2    Mukai, Y.3    Uryu, T.4
  • 44
    • 0017478628 scopus 로고
    • Copolymerization of anhydroglucose and anhydromannose derivatives: Structure, reactivity, and conformational analyses
    • Kobayashi K., Schuerch C. Copolymerization of anhydroglucose and anhydromannose derivatives: structure, reactivity, and conformational analyses. J Polym Sci Polym Chem Ed. 15:1977;913-926.
    • (1977) J Polym Sci Polym Chem Ed , vol.15 , pp. 913-926
    • Kobayashi, K.1    Schuerch, C.2
  • 45
    • 0006640010 scopus 로고
    • Selective synthesis of cellulose-type copolymers by ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives
    • Yoshida T., Song L., Wu C., Hatanaka K., Uryu T. Selective synthesis of cellulose-type copolymers by ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives. Chem Lett. 1991;477-480.
    • (1991) Chem Lett , pp. 477-480
    • Yoshida, T.1    Song, L.2    Wu, C.3    Hatanaka, K.4    Uryu, T.5
  • 46
    • 0031850346 scopus 로고    scopus 로고
    • Two novel synthetic methods for 1,4-anhydro-α-D-xylopyranose derivatives
    • Hori M.F.N. Two novel synthetic methods for 1,4-anhydro-α-D-xylopyranose derivatives. Carbohydr Res. 309:1998;281-286.
    • (1998) Carbohydr Res , vol.309 , pp. 281-286
    • Hori, M.F.N.1
  • 47
    • 0030125905 scopus 로고    scopus 로고
    • Ring-opening polymerization of 1,4-anhydro xylose derivative having an azido group and synthesis of stereoregular 3-amino-3-deoxy-(1→5)-α-D-xylofuranan
    • Yoshida T., Kang B., Hattori K., Qing H., Uryu T. Ring-opening polymerization of 1,4-anhydro xylose derivative having an azido group and synthesis of stereoregular 3-amino-3-deoxy-(1→5)-α-D-xylofuranan. Macromolecules. 29:1996;3117-3122.
    • (1996) Macromolecules , vol.29 , pp. 3117-3122
    • Yoshida, T.1    Kang, B.2    Hattori, K.3    Qing, H.4    Uryu, T.5
  • 48
    • 0343387839 scopus 로고
    • Ring-opening polymerization of cis-3,4-dimethoxyoxolane
    • Thiem J., Haring T. Ring-opening polymerization of cis-3,4-dimethoxyoxolane. Makromol Chem. 188:1987;711-718.
    • (1987) Makromol Chem , vol.188 , pp. 711-718
    • Thiem, J.1    Haring, T.2
  • 49
    • 0342518222 scopus 로고
    • Synthesis and ring-opening polymerization of 1,4:2,5:3,6:-trianhydro-D-mannitol and structure studies by MNDO calculations
    • Strietholt W.A., Thiem J., Howeler U.F.B. Synthesis and ring-opening polymerization of 1,4:2,5:3,6:-trianhydro-D-mannitol and structure studies by MNDO calculations. Makromol Chem. 192:1991;317-331.
    • (1991) Makromol Chem , vol.192 , pp. 317-331
    • Strietholt, W.A.1    Thiem, J.2    Howeler, U.F.B.3
  • 50
    • 0029636657 scopus 로고
    • Regio- And stereospecificity in cationic cyclopolymerization of 1,2:5,6-dianhydro-D-mannitols and synthesis of poly[(1→6)-2,5-anhydro-3,4-di-O-ethyl-D-glucitol]
    • Kakuchi T., Satoh T., Umeda S., Hashimoto H., Yokota K. Regio- and stereospecificity in cationic cyclopolymerization of 1,2:5,6-dianhydro-D-mannitols and synthesis of poly[(1→6)-2,5-anhydro-3,4-di-O-ethyl-D-glucitol]. Macromolecules. 28:1995;4062-4066.
    • (1995) Macromolecules , vol.28 , pp. 4062-4066
    • Kakuchi, T.1    Satoh, T.2    Umeda, S.3    Hashimoto, H.4    Yokota, K.5
  • 51
    • 0000040690 scopus 로고
    • Synthesis of a new macromolecular ionophore with 2,5-anhydro-D-glucitol units via cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-O-ethyl-D-mannitol
    • Hashimoto H., Kakuchi T., Yokota K. Synthesis of a new macromolecular ionophore with 2,5-anhydro-D-glucitol units via cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-O-ethyl-D-mannitol. J Org Chem. 56:1991;6470-6472.
    • (1991) J Org Chem , vol.56 , pp. 6470-6472
    • Hashimoto, H.1    Kakuchi, T.2    Yokota, K.3
  • 52
    • 0000949059 scopus 로고
    • Regio- And stereoselectivity in cationic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-mannitol and -L-iditol and the synthesis of poly[(1→6)-2,5-anhydro-3,4-di-O-methyl-D-glucitol]
    • Kakuchi T., Satoh T., Umeda S., Hashimoto H., Yokota K. Regio- and stereoselectivity in cationic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-mannitol and -L-iditol and the synthesis of poly[(1→6)-2,5-anhydro-3,4-di-O-methyl-D-glucitol]. Macromolecules. 28:1995;5643-5648.
    • (1995) Macromolecules , vol.28 , pp. 5643-5648
    • Kakuchi, T.1    Satoh, T.2    Umeda, S.3    Hashimoto, H.4    Yokota, K.5
  • 53
    • 3342977133 scopus 로고
    • Synthesis of poly[(1→6)-2,5-anhydro-D-glucitol] by cationic cyclopolymerization of 3,4-di-O-allyl-1,2:5,6-dianhydro-D-mannitol
    • Kakuchi T., Umeda S., Satoh T., Hashimoto H., Yokota K. Synthesis of poly[(1→6)-2,5-anhydro-D-glucitol] by cationic cyclopolymerization of 3,4-di-O-allyl-1,2:5,6-dianhydro-D-mannitol. Macromol Rep A. 32:1995;1007-1018.
    • (1995) Macromol Rep a , vol.32 , pp. 1007-1018
    • Kakuchi, T.1    Umeda, S.2    Satoh, T.3    Hashimoto, H.4    Yokota, K.5
  • 54
    • 0030572152 scopus 로고    scopus 로고
    • A novel polymeric carbohydrate. Synthesis of (1→6)-2,5-anhydro-D-glucitol by regio- And stereoselective anionic cyclopolymerization of 1,2:5,6-dianhydro-D-mannitols
    • Satoh T., Hatakeyama T., Umeda S., Hashimoto H., Yokota K., Kakuchi T. A novel polymeric carbohydrate. Synthesis of (1→6)-2,5-anhydro-D-glucitol by regio- and stereoselective anionic cyclopolymerization of 1,2:5,6-dianhydro-D-mannitols. Macromolecules. 29:1996;3447-3452.
    • (1996) Macromolecules , vol.29 , pp. 3447-3452
    • Satoh, T.1    Hatakeyama, T.2    Umeda, S.3    Hashimoto, H.4    Yokota, K.5    Kakuchi, T.6
  • 55
    • 0030573878 scopus 로고    scopus 로고
    • Anionic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-L-iditol leading to (6→1)-2,5-anhydro-3,4-di-O-methyl-D-glucitol]
    • Satoh T., Hatakeyama T., Umeda S., Hashimoto H., Yokota K., Kakuchi T. Anionic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-L-iditol leading to (6→1)-2,5-anhydro-3,4-di-O-methyl-D-glucitol]. Macromolecules. 29:1996;6681-6684.
    • (1996) Macromolecules , vol.29 , pp. 6681-6684
    • Satoh, T.1    Hatakeyama, T.2    Umeda, S.3    Hashimoto, H.4    Yokota, K.5    Kakuchi, T.6
  • 56
    • 0032485681 scopus 로고    scopus 로고
    • Living nature in anionic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-mannitol using the potassium tert-butoxide/18-crown-6 initiating system
    • Hatakeyama T., Kamada M., Satoh T., Yokota K., Kakuchi T. Living nature in anionic cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-mannitol using the potassium tert-butoxide/18-crown-6 initiating system. Macromolecules. 31:1998;2889-2893.
    • (1998) Macromolecules , vol.31 , pp. 2889-2893
    • Hatakeyama, T.1    Kamada, M.2    Satoh, T.3    Yokota, K.4    Kakuchi, T.5
  • 57
    • 0029720979 scopus 로고    scopus 로고
    • Regio- And stereoselective cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-glucitol leading to polymers with 2,5-anhydro-3,4-di-O-methyl-D-mannitol and/or -L-iditol units
    • Satoh T., Hatakeyama T., Umeda S., Yokota K., Kakuchi T. Regio- and stereoselective cyclopolymerization of 1,2:5,6-dianhydro-3,4-di-methyl-D-glucitol leading to polymers with 2,5-anhydro-3,4-di-O-methyl-D-mannitol and/or -L-iditol units. Polym J. 28:1996;520-526.
    • (1996) Polym J , vol.28 , pp. 520-526
    • Satoh, T.1    Hatakeyama, T.2    Umeda, S.3    Yokota, K.4    Kakuchi, T.5
  • 58
    • 0032635237 scopus 로고    scopus 로고
    • Regio- And stereoselective cyclopolymerization of 1,2:5,6-dianhydroallitol and 1,2:5,6-dianhydrogalactitol leading to a novel carbohydrate polymers of (2→6)-1,5-anhydro-D, L-galactitol
    • Kamada M., Satoh T., Yokota K., Kakuchi T. Regio- and stereoselective cyclopolymerization of 1,2:5,6-dianhydroallitol and 1,2:5,6-dianhydrogalactitol leading to a novel carbohydrate polymers of (2→6)-1,5-anhydro-D, L-galactitol. Macromolecules. 32:1999;5755-5759.
    • (1999) Macromolecules , vol.32 , pp. 5755-5759
    • Kamada, M.1    Satoh, T.2    Yokota, K.3    Kakuchi, T.4
  • 59
    • 0028529075 scopus 로고
    • Ring-opening polymerization of 1,4-anhydro-α-D-glucopyranose derivatives having acyl groups and synthesis of (1→5)-β-D-glucofuranan
    • Kamitakahara H., Nakatsubo F., Murakami K. Ring-opening polymerization of 1,4-anhydro-α-D-glucopyranose derivatives having acyl groups and synthesis of (1→5)-β-D-glucofuranan. Macromolecules. 27:1994;5937-5942.
    • (1994) Macromolecules , vol.27 , pp. 5937-5942
    • Kamitakahara, H.1    Nakatsubo, F.2    Murakami, K.3
  • 60
    • 0001379322 scopus 로고    scopus 로고
    • Substituent effect on ring-opening polymerization of regioselectively acylated 1,4-anhydro-α-D-glucopyranose derivatives
    • Kamitakahara H., Nakatsuo F. Substituent effect on ring-opening polymerization of regioselectively acylated 1,4-anhydro-α-D-glucopyranose derivatives. Macromolecules. 29:1996;1119-1122.
    • (1996) Macromolecules , vol.29 , pp. 1119-1122
    • Kamitakahara, H.1    Nakatsuo, F.2
  • 62
    • 0029927722 scopus 로고    scopus 로고
    • Cationic ring-opening polymerization of 3,6-di-O-benzyl-α-D-glucose 1,2,4-orthopivalate and the first chemical synthesis of cellulose
    • Nakatsubo F., Kamitakahara H., Horii M. Cationic ring-opening polymerization of 3,6-di-O-benzyl-α-D-glucose 1,2,4-orthopivalate and the first chemical synthesis of cellulose. J Am Chem Soc. 118:1996;1677-1681.
    • (1996) J Am Chem Soc , vol.118 , pp. 1677-1681
    • Nakatsubo, F.1    Kamitakahara, H.2    Horii, M.3
  • 63
    • 0030576777 scopus 로고    scopus 로고
    • Substituent effect on ring-opening polymerization of regioselectively acylated α-D-glucopyranose 1,2,4-orthopivalate derivatives
    • Kamitakahara H., Horie M., Nakatsubo F. Substituent effect on ring-opening polymerization of regioselectively acylated α-D-glucopyranose 1,2,4-orthopivalate derivatives. Macromolecules. 29:1996;6126-6131.
    • (1996) Macromolecules , vol.29 , pp. 6126-6131
    • Kamitakahara, H.1    Horie, M.2    Nakatsubo, F.3
  • 64
    • 0031147251 scopus 로고    scopus 로고
    • Substituent effect of the orthoester group on ring-opening polymerization of α-D-glucopyranose 1,2,4-orthoester derivatives
    • Hori M., Kamitakahara H., Nakatsubo F. Substituent effect of the orthoester group on ring-opening polymerization of α-D-glucopyranose 1,2,4-orthoester derivatives. Macromolecules. 30:1997;2891-2896.
    • (1997) Macromolecules , vol.30 , pp. 2891-2896
    • Hori, M.1    Kamitakahara, H.2    Nakatsubo, F.3
  • 65
    • 0032052501 scopus 로고    scopus 로고
    • A novel synthetic method for α-D-galactofuranose 1,2,5-orthopivalate
    • Tsujihata S., Nakatsubo F. A novel synthetic method for α-D-galactofuranose 1,2,5-orthopivalate. Carbohydr Res. 308:1998;439-443.
    • (1998) Carbohydr Res , vol.308 , pp. 439-443
    • Tsujihata, S.1    Nakatsubo, F.2
  • 66
    • 0002713695 scopus 로고
    • Synthetic studies of cellulose X. Selection of suitable starting materials for the convergent synthesis of cello-oligo-saccharides
    • Nishimura T., Takano T., Nakatsubo F., Murakami K. Synthetic studies of cellulose X. Selection of suitable starting materials for the convergent synthesis of cello-oligo-saccharides. Mokuzai Gakkai-shi. 39:1993;40-47.
    • (1993) Mokuzai Gakkai-shi , vol.39 , pp. 40-47
    • Nishimura, T.1    Takano, T.2    Nakatsubo, F.3    Murakami, K.4
  • 67
  • 68
    • 0030590993 scopus 로고    scopus 로고
    • First stepwise synthesis of cellulose analogs
    • Nishimura T., Nakatsubo F. First stepwise synthesis of cellulose analogs. Tetrahedron Lett. 37:1996;9215-9218.
    • (1996) Tetrahedron Lett , vol.37 , pp. 9215-9218
    • Nishimura, T.1    Nakatsubo, F.2
  • 69
    • 0000594912 scopus 로고    scopus 로고
    • Chemical synthesis of cellulose derivatives by a convergent synthetic method and several of their properties
    • Nishimura T., Nakatsubo F. Chemical synthesis of cellulose derivatives by a convergent synthetic method and several of their properties. Cellulose. 4:1997;109-130.
    • (1997) Cellulose , vol.4 , pp. 109-130
    • Nishimura, T.1    Nakatsubo, F.2
  • 70
    • 0003458664 scopus 로고
    • K. Drauz, Waldmann H. Weinheim: VCH
    • Drauz K., Waldmann H. Enzyme catalysis in organic synthesis. vols. 1 and 2:1995;VCH, Weinheim.
    • (1995) Enzyme Catalysis in Organic Synthesis , vol.12
  • 71
    • 0001981056 scopus 로고
    • Enzymatic polymerization and oligomerization
    • Kobayashi S., Shoda S., Uyama U. Enzymatic polymerization and oligomerization. Adv Polym Sci. 121:1995;1-30.
    • (1995) Adv Polym Sci , vol.121 , pp. 1-30
    • Kobayashi, S.1    Shoda, S.2    Uyama, U.3
  • 72
    • 0032592234 scopus 로고    scopus 로고
    • Enzymatic polymerization: A new method of polymer synthesis
    • Kobayashi S. Enzymatic polymerization: a new method of polymer synthesis. J Polym Sci A Polym Chem. 37:1999;3041-3056.
    • (1999) J Polym Sci a Polym Chem , vol.37 , pp. 3041-3056
    • Kobayashi, S.1
  • 73
    • 0001547441 scopus 로고
    • Novel method for polysaccharide synthesis using an enzyme: The first in vitro synthesis of cellulose via a nonbiosynthetic path utilizing cellulase as catalyst
    • Kobayashi S., Kashiwa K., Kawasaki T., Shoda S. Novel method for polysaccharide synthesis using an enzyme: the first in vitro synthesis of cellulose via a nonbiosynthetic path utilizing cellulase as catalyst. J Am Chem Soc. 113:1991;3079-3084.
    • (1991) J Am Chem Soc , vol.113 , pp. 3079-3084
    • Kobayashi, S.1    Kashiwa, K.2    Kawasaki, T.3    Shoda, S.4
  • 74
    • 0027115081 scopus 로고
    • Enzymatic polymerization of α-D-maltosyl fluoride utilizing α-amylase as the catalyst: A new approach for the synthesis of maltooligosaccharides
    • Kobayashi S., Shimada J., Kashiwa K., Shoda S. Enzymatic polymerization of α-D-maltosyl fluoride utilizing α-amylase as the catalyst: a new approach for the synthesis of maltooligosaccharides. Macromolecules. 25:1992;3237-3241.
    • (1992) Macromolecules , vol.25 , pp. 3237-3241
    • Kobayashi, S.1    Shimada, J.2    Kashiwa, K.3    Shoda, S.4
  • 75
    • 0030105865 scopus 로고    scopus 로고
    • Specific preparation of artificial xylan: A new approach to polysaccharides synthesis by using cellulase as catalyst
    • Kobayashi S., Wen X., Shoda S. Specific preparation of artificial xylan: a new approach to polysaccharides synthesis by using cellulase as catalyst. Macromolecules. 29:1996;2698-2700.
    • (1996) Macromolecules , vol.29 , pp. 2698-2700
    • Kobayashi, S.1    Wen, X.2    Shoda, S.3
  • 76
    • 0031585039 scopus 로고    scopus 로고
    • A novel method for synthesis of chitobiose via enzymatic glycosylation using a sugar oxazoline as glycosyl donor
    • Kobayashi S., Kiyosada T., Shoda S. A novel method for synthesis of chitobiose via enzymatic glycosylation using a sugar oxazoline as glycosyl donor. Tetrahedron Lett. 38:1997;2111-2112.
    • (1997) Tetrahedron Lett , vol.38 , pp. 2111-2112
    • Kobayashi, S.1    Kiyosada, T.2    Shoda, S.3
  • 77
    • 0030452755 scopus 로고    scopus 로고
    • Synthesis of artificial chitin: Irreversible catalytic behavior of a glycosyl hydrolase through a transition state analogue substrate
    • Kobayashi S., Kiyosada T., Shoda S. Synthesis of artificial chitin: irreversible catalytic behavior of a glycosyl hydrolase through a transition state analogue substrate. J Am Chem Soc. 118:1996;13,113-13,114.
    • (1996) J Am Chem Soc , vol.118 , pp. 13
    • Kobayashi, S.1    Kiyosada, T.2    Shoda, S.3
  • 79
    • 0032650475 scopus 로고    scopus 로고
    • Chemical synthesis of as amylose-like polysaccharide by polymerization of partially benzylated 1-thio-β-maltooctaoside derived from gamma-cyclodextrin
    • Nishiki M., Ousaka Y., Nishi N., Tokura S., Sakairi N. Chemical synthesis of as amylose-like polysaccharide by polymerization of partially benzylated 1-thio-β-maltooctaoside derived from gamma-cyclodextrin. Carbohydr Polym. 39:1999;1-6.
    • (1999) Carbohydr Polym , vol.39 , pp. 1-6
    • Nishiki, M.1    Ousaka, Y.2    Nishi, N.3    Tokura, S.4    Sakairi, N.5
  • 80
    • 37049073503 scopus 로고
    • Modification of cyclodextrins by insertion of a heterogeneous sugar unit into their skeletons. Synthesis of 2-amino-2-deoxy-β-cyclodextrin from α-cyclodextrin
    • Sakairi N., Wang L., Kuzuhara H. Modification of cyclodextrins by insertion of a heterogeneous sugar unit into their skeletons. Synthesis of 2-amino-2-deoxy-β-cyclodextrin from α-cyclodextrin. J Chem Soc Perkin Trans 1. 1995;437-443.
    • (1995) J Chem Soc Perkin Trans 1 , pp. 437-443
    • Sakairi, N.1    Wang, L.2    Kuzuhara, H.3
  • 81
    • 0002182380 scopus 로고
    • Polymerization of a cellobiose derivative to comb-shaped oligosaccharides
    • Masura V., Schuerch C. Polymerization of a cellobiose derivative to comb-shaped oligosaccharides. Carbohydr Res. 15:1972;65-72.
    • (1972) Carbohydr Res , vol.15 , pp. 65-72
    • Masura, V.1    Schuerch, C.2
  • 82
    • 0000338994 scopus 로고
    • The preparation of comb-shaped polysaccharides by polymerization of a maltose derivative
    • Veruovic B., Schuerch C. The preparation of comb-shaped polysaccharides by polymerization of a maltose derivative. Carbohydr Res. 14:1970;199-206.
    • (1970) Carbohydr Res , vol.14 , pp. 199-206
    • Veruovic, B.1    Schuerch, C.2
  • 83
    • 0015636681 scopus 로고
    • Copolymerization of 1,6-anhydroglucose and 1,6-anhydromaltose derivatives
    • Lindenberger W.H., Schuerch C. Copolymerization of 1,6-anhydroglucose and 1,6-anhydromaltose derivatives. J Polym Sci Polym Chem Ed. 11:1973;1225-1235.
    • (1973) J Polym Sci Polym Chem Ed , vol.11 , pp. 1225-1235
    • Lindenberger, W.H.1    Schuerch, C.2
  • 84
    • 0027911157 scopus 로고
    • Chemical synthesis of a comb-shaped branched stereoregular polysaccharide, 4-O-α-D-mannopyranosyl-(1→6)-α-D-mannopyranan
    • Kobayashi K., Nomura K., Okada M. Chemical synthesis of a comb-shaped branched stereoregular polysaccharide, 4-O-α-D-mannopyranosyl-(1→6)-α-D-mannopyranan. Carbohydr Res. 242:1993;161-166.
    • (1993) Carbohydr Res , vol.242 , pp. 161-166
    • Kobayashi, K.1    Nomura, K.2    Okada, M.3
  • 85
    • 84986794843 scopus 로고
    • Cationic ring-opening polymerization of new 1,6-anhydro-β-lactose derivatives
    • Yoshida T., Yasuda Y., Hattori K., Uryu T. Cationic ring-opening polymerization of new 1,6-anhydro-β-lactose derivatives. Macromol Rapid Commun. 16:1995;881-890.
    • (1995) Macromol Rapid Commun , vol.16 , pp. 881-890
    • Yoshida, T.1    Yasuda, Y.2    Hattori, K.3    Uryu, T.4
  • 86
    • 0342952359 scopus 로고    scopus 로고
    • Cationic ring-opening polymerization of 1,6-anhydro-β-D-lactose derivatives
    • Kanematsu Y., Yoshida T. Cationic ring-opening polymerization of 1,6-anhydro-β-D-lactose derivatives. Polym Prepr Jpn. 45:1996;1429-1430.
    • (1996) Polym Prepr Jpn , vol.45 , pp. 1429-1430
    • Kanematsu, Y.1    Yoshida, T.2
  • 87
    • 0343387836 scopus 로고    scopus 로고
    • Synthesis of new branched polysaccharides by cationic ring-opening polymerization of anhydro ribo-disaccharide derivative
    • 3pp.
    • Endo K, Yoshida T. Synthesis of new branched polysaccharides by cationic ring-opening polymerization of anhydro ribo-disaccharide derivative. Abstr 73th Chem Soc Jpn, 1997. 3pp.
    • (1997) Abstr 73th Chem Soc Jpn
    • Endo, K.1    Yoshida, T.2
  • 88
    • 0343823464 scopus 로고    scopus 로고
    • Synthesis of branched polysaccharides by ring-opening polymerization of 1,4-anhydro-ribo-oligosaccharides
    • Endo K., Yoshida T. Synthesis of branched polysaccharides by ring-opening polymerization of 1,4-anhydro-ribo-oligosaccharides. Polym Prepr Jpn. 47:1998;221.
    • (1998) Polym Prepr Jpn , vol.47 , pp. 221
    • Endo, K.1    Yoshida, T.2
  • 89
    • 0025401595 scopus 로고
    • Synthesis of a comb-shaped branched polysaccharide via ring-opening polymerization of a reactive anhydro disaccharide derivative
    • Ichikawa H., Kobayashi K., Sumitomo H. Synthesis of a comb-shaped branched polysaccharide via ring-opening polymerization of a reactive anhydro disaccharide derivative. Macromolecules. 23:1990;1884-1886.
    • (1990) Macromolecules , vol.23 , pp. 1884-1886
    • Ichikawa, H.1    Kobayashi, K.2    Sumitomo, H.3
  • 90
    • 0032564629 scopus 로고    scopus 로고
    • The chemical synthesis of a cyclic oligosaccharide derivative with branching
    • Kasuya M.C., Hatanaka K. The chemical synthesis of a cyclic oligosaccharide derivative with branching. Tetrahedron Lett. 39:1998;9719-9722.
    • (1998) Tetrahedron Lett , vol.39 , pp. 9719-9722
    • Kasuya, M.C.1    Hatanaka, K.2
  • 91
    • 0010918285 scopus 로고
    • Synthesis of α-(1→3)-branched dextrans by copolymerization and α-D-glucosidation
    • Ito H., Schuerch C. Synthesis of α-(1→3)-branched dextrans by copolymerization and α-D-glucosidation. J Am Chem Soc. 101:1979;5797-5806.
    • (1979) J Am Chem Soc , vol.101 , pp. 5797-5806
    • Ito, H.1    Schuerch, C.2
  • 92
    • 0011409967 scopus 로고
    • Ring-opening polymerization of 1,6-anhydro-2,4-di-O-benzyl-3-O-tert-butyldimethylsilyl-β-D-gluco-pyranose and synthesis of α-(1→3)-branched dextrans
    • Uryu T., Yamanaka M., Henmi M., Hatanaka K., Matsuzaki K. Ring-opening polymerization of 1,6-anhydro-2,4-di-O-benzyl-3-O-tert-butyldimethylsilyl-β-D-gluco-pyranose and synthesis of α-(1→3)-branched dextrans. Carbohydr Res. 157:1986;157-169.
    • (1986) Carbohydr Res , vol.157 , pp. 157-169
    • Uryu, T.1    Yamanaka, M.2    Henmi, M.3    Hatanaka, K.4    Matsuzaki, K.5
  • 94
    • 0006640010 scopus 로고
    • Selective synthesis of cellulose-type copolymers by ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives
    • Yoshida T., Song L., Wu C., Hatanaka K., Uryu T. Selective synthesis of cellulose-type copolymers by ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives. Chem Lett. 1991;477-480.
    • (1991) Chem Lett , pp. 477-480
    • Yoshida, T.1    Song, L.2    Wu, C.3    Hatanaka, K.4    Uryu, T.5
  • 95
    • 0028485705 scopus 로고
    • Synthesis of cellulose-type polyriboses and their branched sulfates with anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives
    • Yoshida T., Wu C., Song L., Uryu T., Kaneko Y., Mimura T., Nakashima H., Yamamoto N. Synthesis of cellulose-type polyriboses and their branched sulfates with anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives. Macromolecules. 27:1994;4422-4428.
    • (1994) Macromolecules , vol.27 , pp. 4422-4428
    • Yoshida, T.1    Wu, C.2    Song, L.3    Uryu, T.4    Kaneko, Y.5    Mimura, T.6    Nakashima, H.7    Yamamoto, N.8
  • 96
    • 0027110844 scopus 로고
    • Synthesis of branched ribofuranans and their sulfates with strong anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives
    • Yoshida T., Katayama Y., Inoue S., Uryu T. Synthesis of branched ribofuranans and their sulfates with strong anti-AIDS virus activity by selective ring-opening copolymerization of 1,4-anhydro-α-D-ribopyranose derivatives. Macromolecules. 25:1992;4051-4057.
    • (1992) Macromolecules , vol.25 , pp. 4051-4057
    • Yoshida, T.1    Katayama, Y.2    Inoue, S.3    Uryu, T.4
  • 97
    • 0009264075 scopus 로고
    • Synthesis of water-soluble branched polysaccharides and their antitumor activity, 1. Branched polysaccharides from cellulose acetate
    • Matsuzaki K., Yamamoto I., Sato T., Oshima R. Synthesis of water-soluble branched polysaccharides and their antitumor activity, 1. Branched polysaccharides from cellulose acetate. Makromol Chem. 186:1985;449-456.
    • (1985) Makromol Chem , vol.186 , pp. 449-456
    • Matsuzaki, K.1    Yamamoto, I.2    Sato, T.3    Oshima, R.4
  • 99
    • 0009020899 scopus 로고
    • Synthesis of water-soluble polysaccharides and their antitumor activity, 2. Branched polysaccharides from curdlan and curdlan acetate
    • Matsuzaki K., Yamamoto I., Sato T., Oshima R. Synthesis of water-soluble polysaccharides and their antitumor activity, 2. Branched polysaccharides from curdlan and curdlan acetate. Makromol Chem. 187:1986;317-324.
    • (1986) Makromol Chem , vol.187 , pp. 317-324
    • Matsuzaki, K.1    Yamamoto, I.2    Sato, T.3    Oshima, R.4
  • 100
    • 0000661459 scopus 로고
    • Synthesis and in vitro inhibitory effect of L-glycosyl-branched curdlan sulfates on AIDS virus infection
    • Yoshida T., Yasuda Y., Uryu T., Nakashima H., Yamamoto N., Mimura T., Kaneko Y. Synthesis and in vitro inhibitory effect of L-glycosyl-branched curdlan sulfates on AIDS virus infection. Macromolecules. 27:1994;6272-6276.
    • (1994) Macromolecules , vol.27 , pp. 6272-6276
    • Yoshida, T.1    Yasuda, Y.2    Uryu, T.3    Nakashima, H.4    Yamamoto, N.5    Mimura, T.6    Kaneko, Y.7
  • 101
    • 0000232363 scopus 로고
    • Chemical synthesis of amino-group-containing (1→6)-α-D-glucan derivatives by ring-opening polymerization of 1,6-anhydro-azido sugars
    • Uryu T., Hatanaka K., Matsuzaki K., Kuzuhara H. Chemical synthesis of amino-group-containing (1→6)-α-D-glucan derivatives by ring-opening polymerization of 1,6-anhydro-azido sugars. Macromolecules. 16:1983;853-858.
    • (1983) Macromolecules , vol.16 , pp. 853-858
    • Uryu, T.1    Hatanaka, K.2    Matsuzaki, K.3    Kuzuhara, H.4
  • 102
    • 0020800134 scopus 로고
    • Synthesis and stereoregular hetero polysaccharides having amino-groups by ring-opening copolymerization of 1,6-anhydro-azido-sugar derivatives
    • Uryu T., Hatanaka K., Matsuzaki K. Synthesis and stereoregular hetero polysaccharides having amino-groups by ring-opening copolymerization of 1,6-anhydro-azido-sugar derivatives. J Polym Sci Polym Chem Ed. 21:1983;2203-2214.
    • (1983) J Polym Sci Polym Chem Ed , vol.21 , pp. 2203-2214
    • Uryu, T.1    Hatanaka, K.2    Matsuzaki, K.3
  • 104
    • 0012262528 scopus 로고    scopus 로고
    • Ring-opening polymerization and copolymerization of a new benzylated 1,6-anhydro-3-azido-3-deoxy-β-D-allopyranose and synthesis of amino-polysaccharides with 1,6-α-allopyranosidic structure
    • Hattori K., Yoshida T., Uryu T. Ring-opening polymerization and copolymerization of a new benzylated 1,6-anhydro-3-azido-3-deoxy-β-D-allopyranose and synthesis of amino-polysaccharides with 1,6-α-allopyranosidic structure. Macromol Chem Phys. 198:1997;29-39.
    • (1997) Macromol Chem Phys , vol.198 , pp. 29-39
    • Hattori, K.1    Yoshida, T.2    Uryu, T.3
  • 105
    • 0032114833 scopus 로고    scopus 로고
    • Ring-opening polymerization of new 1,6-anhydro-β-D-glucosamine derivatives
    • Hattori K., Yoshida T., Uryu T. Ring-opening polymerization of new 1,6-anhydro-β-D-glucosamine derivatives. Carbohydr Polym. 36:1998;129-135.
    • (1998) Carbohydr Polym , vol.36 , pp. 129-135
    • Hattori, K.1    Yoshida, T.2    Uryu, T.3
  • 106
    • 0038493022 scopus 로고    scopus 로고
    • Synthesis of 3-amino-ribofuranans having 1,5-α And -β structures by selective ring-opening polymerization of a 1,4-anhydro-3-azido-3-deoxy-α-D-ribopyranose derivative
    • Kang B., Hattori K., Yoshida T., Hirai M., Choi Y., Uryu T. Synthesis of 3-amino-ribofuranans having 1,5-α and -β structures by selective ring-opening polymerization of a 1,4-anhydro-3-azido-3-deoxy-α-D-ribopyranose derivative. Macromol Chem Phys. 198:1997;1331-1345.
    • (1997) Macromol Chem Phys , vol.198 , pp. 1331-1345
    • Kang, B.1    Hattori, K.2    Yoshida, T.3    Hirai, M.4    Choi, Y.5    Uryu, T.6
  • 107
    • 0032138594 scopus 로고    scopus 로고
    • Synthesis of 3-acetamido-3-deoxy-(1→5)-α-D-xylofuranan by ring-opening polymerization of a 1,4-anhydro-3-azido-α-D-xylopyranose derivative
    • Borjihan G., Uryu T. Synthesis of 3-acetamido-3-deoxy-(1→5)-α-D-xylofuranan by ring-opening polymerization of a 1,4-anhydro-3-azido-α-D-xylopyranose derivative. Macromolecules. 31:1998;5572-5576.
    • (1998) Macromolecules , vol.31 , pp. 5572-5576
    • Borjihan, G.1    Uryu, T.2
  • 108
    • 0032685886 scopus 로고    scopus 로고
    • Synthesis of 3-acetamido-3-deoxy-(1→5)-α-D-ribofuranan by ring-opening polymerization of 1,4-anhydro-3-azido-α-D-ribopyranose derivative
    • Borjihan G., Okuyama K., Katsuraya K., Uryu T. Synthesis of 3-acetamido-3-deoxy-(1→5)-α-D-ribofuranan by ring-opening polymerization of 1,4-anhydro-3-azido-α-D-ribopyranose derivative. Polym J. 31:1999;167-171.
    • (1999) Polym J , vol.31 , pp. 167-171
    • Borjihan, G.1    Okuyama, K.2    Katsuraya, K.3    Uryu, T.4
  • 109
    • 0021855447 scopus 로고
    • Synthesis and functions of polystyrene derivatives having pendant oligosaccharides
    • Kobayashi K., Sumitomo H., Ina Y. Synthesis and functions of polystyrene derivatives having pendant oligosaccharides. Polym J. 17:1985;567-575.
    • (1985) Polym J , vol.17 , pp. 567-575
    • Kobayashi, K.1    Sumitomo, H.2    Ina, Y.3
  • 110
    • 0020938564 scopus 로고
    • A carbohydrate-containing synthetic polymer obtained from N-p-vinylbenzyl-D-gluconamide
    • Kobayashi K., Sumitomo H., Ina Y. A carbohydrate-containing synthetic polymer obtained from N-p-vinylbenzyl-D-gluconamide. Polym J. 15:1983;667-671.
    • (1983) Polym J , vol.15 , pp. 667-671
    • Kobayashi, K.1    Sumitomo, H.2    Ina, Y.3
  • 111
    • 0042189552 scopus 로고
    • Maltopentaose- And maltoheptaose-carrying styrene macromers and their homopolymers
    • Kobayashi K., Sumitomo H., Itoigawa T. Maltopentaose- and maltoheptaose-carrying styrene macromers and their homopolymers. Macromolecules. 20:1987;906-908.
    • (1987) Macromolecules , vol.20 , pp. 906-908
    • Kobayashi, K.1    Sumitomo, H.2    Itoigawa, T.3
  • 112
    • 84986793496 scopus 로고
    • Chemoenzymatic synthesis of polymerizable 11-methacryloylaminoundecanoic ester of 1- And 3-O-methyl-α-D-glucose in 6-O-position
    • Geyer U., Klemm D., Pavel K., Ritter H. Chemoenzymatic synthesis of polymerizable 11-methacryloylaminoundecanoic ester of 1- and 3-O-methyl-α-D-glucose in 6-O-position. Macromol Rapid Commun. 16:1995;337-341.
    • (1995) Macromol Rapid Commun , vol.16 , pp. 337-341
    • Geyer, U.1    Klemm, D.2    Pavel, K.3    Ritter, H.4
  • 113
    • 0030871550 scopus 로고    scopus 로고
    • Controlled synthesis of amphiphilic block copolymers with pendant glucose residues by living cationic polymerization
    • Yamada K., Minoda M., Miyamoto T. Controlled synthesis of amphiphilic block copolymers with pendant glucose residues by living cationic polymerization. J Polym Sci A Polym Chem. 35:1997;255-261.
    • (1997) J Polym Sci a Polym Chem , vol.35 , pp. 255-261
    • Yamada, K.1    Minoda, M.2    Miyamoto, T.3
  • 114
    • 0032652697 scopus 로고    scopus 로고
    • Controlled synthesis of amphiphilic block copolymers with pendant N-acetyl-D-glucosamine residues by living cationic polymerization and their interaction with WGA lectin
    • Yamada K., Minoda M., Miyamoto T. Controlled synthesis of amphiphilic block copolymers with pendant N-acetyl-D-glucosamine residues by living cationic polymerization and their interaction with WGA lectin. Macromolecules. 32:1999;3553-3558.
    • (1999) Macromolecules , vol.32 , pp. 3553-3558
    • Yamada, K.1    Minoda, M.2    Miyamoto, T.3
  • 115
    • 0031103538 scopus 로고    scopus 로고
    • Controlled synthesis of glycopolymers with pendant D-glucosamine residues by living cationic polymerization
    • Yamada K., Minoda M., Miyamoto T. Controlled synthesis of glycopolymers with pendant D-glucosamine residues by living cationic polymerization. J Polym Sci A Polym Chem. 35:1997;751-757.
    • (1997) J Polym Sci a Polym Chem , vol.35 , pp. 751-757
    • Yamada, K.1    Minoda, M.2    Miyamoto, T.3
  • 116
    • 0028455010 scopus 로고
    • Synthesis of nonionic and anionic hydrogels bearing a monosaccharide residue and their properties
    • Fukudome N., Suzuki K., Yashima E., Akashi M. Synthesis of nonionic and anionic hydrogels bearing a monosaccharide residue and their properties. J Appl Polym Sci. 52:1994;1759-1763.
    • (1994) J Appl Polym Sci , vol.52 , pp. 1759-1763
    • Fukudome, N.1    Suzuki, K.2    Yashima, E.3    Akashi, M.4
  • 117
    • 0001688950 scopus 로고
    • Protective effect of seaweed extracts for chicken embryos infected with influenza B or mumps virus
    • Gerber P., Dutcher J.D., Adams E.V., Sherman J.H. Protective effect of seaweed extracts for chicken embryos infected with influenza B or mumps virus. Proc Soc Exp Biol Med. 99:1958;590-593.
    • (1958) Proc Soc Exp Biol Med , vol.99 , pp. 590-593
    • Gerber, P.1    Dutcher, J.D.2    Adams, E.V.3    Sherman, J.H.4
  • 118
    • 0000337276 scopus 로고
    • Effect of synthetic and biological polyanions on herpes simplex virus
    • Nahmias J., Kibrick S., Bernfeld P. Effect of synthetic and biological polyanions on herpes simplex virus. Proc Soc Exp Biol Med. 115:1964;993-996.
    • (1964) Proc Soc Exp Biol Med , vol.115 , pp. 993-996
    • Nahmias, J.1    Kibrick, S.2    Bernfeld, P.3
  • 119
    • 84872446632 scopus 로고
    • Inhibition of herpes virus by natural and synthetic acid polysaccharides
    • Takemoto K.K., Fabisch P. Inhibition of herpes virus by natural and synthetic acid polysaccharides. Proc Soc Exp Biol Med. 116:1964;114-140.
    • (1964) Proc Soc Exp Biol Med , vol.116 , pp. 114-140
    • Takemoto, K.K.1    Fabisch, P.2
  • 120
    • 0023274352 scopus 로고
    • Dextran sulfate, a potent anti-HIV agent in vitro having synergism with zidovudine
    • Ueno R., Kuno S. Dextran sulfate, a potent anti-HIV agent in vitro having synergism with zidovudine. Lancet. 1987;1379.
    • (1987) Lancet , pp. 1379
    • Ueno, R.1    Kuno, S.2
  • 122
    • 0025186450 scopus 로고
    • Molecular targets for AIDS therapy
    • Mitsuya H., Yarchoan R., Broder S. Molecular targets for AIDS therapy. Science. 249:1990;1533-1544.
    • (1990) Science , vol.249 , pp. 1533-1544
    • Mitsuya, H.1    Yarchoan, R.2    Broder, S.3
  • 123
    • 0041688028 scopus 로고
    • Regulation of the blood coagulation mechanism by anticoagulantly active heparan sulfate proteoglycans
    • V. Ginsberg, & P.W. Robbins. London: JAI Press
    • Morcam J.A., Rosenberg R.D. Regulation of the blood coagulation mechanism by anticoagulantly active heparan sulfate proteoglycans. Ginsberg V., Robbins P.W. Biology of carbohydrates. 1991;47-74 JAI Press, London.
    • (1991) Biology of Carbohydrates , pp. 47-74
    • Morcam, J.A.1    Rosenberg, R.D.2
  • 124
    • 0001916332 scopus 로고
    • D.A. Lane, & U. Lindahl. London: KABI Service
    • Lane D.A., Lindahl U. Heparin. 1989;KABI Service, London.
    • (1989) Heparin
  • 127
    • 0342518204 scopus 로고
    • US Pharmacopoeia National Formulary. USP XXI
    • US Pharmacopoeia National Formulary. USP XXI, 1985. p. 480-3.
    • (1985) , pp. 480-483
  • 128
  • 130
    • 0028085580 scopus 로고
    • A phase I study of curdlan sulfonate an HIV inhibitor. Tolerance, pharmacokinetics and effects on coagulation and on CD4 lymphocytes
    • Gordon M., Guralnik M., Kaneko Y., Mimura T., Baker M., Lang T. A phase I study of curdlan sulfonate an HIV inhibitor. Tolerance, pharmacokinetics and effects on coagulation and on CD4 lymphocytes. J Med. 25:1994;163-179.
    • (1994) J Med , vol.25 , pp. 163-179
    • Gordon, M.1    Guralnik, M.2    Kaneko, Y.3    Mimura, T.4    Baker, M.5    Lang, T.6
  • 131
    • 0343387815 scopus 로고
    • In search of AIDS-resistance genes
    • O'Brien S.J., Dean M. In search of AIDS-resistance genes. Sci Am. 1995;28-35.
    • (1995) Sci Am , pp. 28-35
    • O'Brien, S.J.1    Dean, M.2
  • 133
    • 0028970837 scopus 로고    scopus 로고
    • Synthesis of curdlan sulfates having inhibitory effects in vitro against AIDS viruses HIV-1 and HIV-2
    • Yoshida T., Yasuda Y., Mimura T., Kaneko Y., Nakashima H., Yamamoto N., Uryu T. Synthesis of curdlan sulfates having inhibitory effects in vitro against AIDS viruses HIV-1 and HIV-2. Carbohydr Res. 276:1996;425-436.
    • (1996) Carbohydr Res , vol.276 , pp. 425-436
    • Yoshida, T.1    Yasuda, Y.2    Mimura, T.3    Kaneko, Y.4    Nakashima, H.5    Yamamoto, N.6    Uryu, T.7
  • 136
    • 0031557636 scopus 로고    scopus 로고
    • Studies on interaction mechanism of sulfonated polysaccharides as an AIDS drug by NMR
    • Jeon K., Katsuraya K., Kaneko Y., Mimura T., Uryu T. Studies on interaction mechanism of sulfonated polysaccharides as an AIDS drug by NMR. Macromolecules. 30:1997;1997-2001.
    • (1997) Macromolecules , vol.30 , pp. 1997-2001
    • Jeon, K.1    Katsuraya, K.2    Kaneko, Y.3    Mimura, T.4    Uryu, T.5
  • 137
    • 0027841942 scopus 로고
    • Anti-AIDS virus activity in vitro of dextran sulfates obtained by sulfation of synthetic and natural dextrans
    • Yoshida T., Nakashima H., Yamamoto N., Uryu T. Anti-AIDS virus activity in vitro of dextran sulfates obtained by sulfation of synthetic and natural dextrans. Polym J. 25:1993;1069-1077.
    • (1993) Polym J , vol.25 , pp. 1069-1077
    • Yoshida, T.1    Nakashima, H.2    Yamamoto, N.3    Uryu, T.4
  • 138
    • 5344241356 scopus 로고
    • Effect of degree of sulfonation on anti-HIV activity of synthetic (1→5)-α-D-ribofuranan sulfate
    • Hatanaka K., Nakajima I., Yoshida T., Uryu T., Yoshida O., Yamamoto N. Effect of degree of sulfonation on anti-HIV activity of synthetic (1→5)-α-D-ribofuranan sulfate. J Carbohydr Chem. 10:1991;681-690.
    • (1991) J Carbohydr Chem , vol.10 , pp. 681-690
    • Hatanaka, K.1    Nakajima, I.2    Yoshida, T.3    Uryu, T.4    Yoshida, O.5    Yamamoto, N.6
  • 139
    • 0030043854 scopus 로고    scopus 로고
    • Synthesis of sulfated octadecyl ribo-oligosaccharides with potent anti-AIDS virus activity by ring-opening polymerization of a 1,4-anhydroribose derivative
    • Choi Y., Yoshida T., Mimura T., Kaneko Y., Nakashima H., Yamamoto N., Uryu T. Synthesis of sulfated octadecyl ribo-oligosaccharides with potent anti-AIDS virus activity by ring-opening polymerization of a 1,4-anhydroribose derivative. Carbohydr Res. 282:1996;113-123.
    • (1996) Carbohydr Res , vol.282 , pp. 113-123
    • Choi, Y.1    Yoshida, T.2    Mimura, T.3    Kaneko, Y.4    Nakashima, H.5    Yamamoto, N.6    Uryu, T.7
  • 140
    • 0030647813 scopus 로고    scopus 로고
    • Synthesis of sulfated deoxy-ribofuranans having selective anti-AIDS virus activity by ring-opening copolymerization of 1,4-anhydro ribose derivatives
    • Choi Y., Kang B., Lu R., Osawa M., Hattori K., Yoshida T., Mimura T., Kaneko Y., Nakashima H., Yamamoto N., Uryu T. Synthesis of sulfated deoxy-ribofuranans having selective anti-AIDS virus activity by ring-opening copolymerization of 1,4-anhydro ribose derivatives. Polym J. 29:1997;374-379.
    • (1997) Polym J , vol.29 , pp. 374-379
    • Choi, Y.1    Kang, B.2    Lu, R.3    Osawa, M.4    Hattori, K.5    Yoshida, T.6    Mimura, T.7    Kaneko, Y.8    Nakashima, H.9    Yamamoto, N.10    Uryu, T.11
  • 144
    • 0342518203 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of sulfated polysaccharides containing acetamido groups
    • Borjihan G., Katsuraya K., Nakashima H., Uryu T. Synthesis and anti-HIV activity of sulfated polysaccharides containing acetamido groups. Sen'i Gakkai-shi. 55:1999;323-330.
    • (1999) Sen'i Gakkai-shi , vol.55 , pp. 323-330
    • Borjihan, G.1    Katsuraya, K.2    Nakashima, H.3    Uryu, T.4
  • 153
    • 0029370191 scopus 로고
    • Urushi (oriental lacquer) a natural aesthetic durable and future-promising coating
    • Kumanotani J. Urushi (oriental lacquer) a natural aesthetic durable and future-promising coating. Prog Org Coatings. 26:1995;163-195.
    • (1995) Prog Org Coatings , vol.26 , pp. 163-195
    • Kumanotani, J.1
  • 154
    • 1942517138 scopus 로고
    • Studies on the urushi (the latex of the lacquer tree). Part 1. Comparison between the latex of the Burmese lacquer tree and the latex of the Japanese lacquer tree
    • Oda Y., Ishida T., Honnda K. Studies on the urushi (the latex of the lacquer tree). Part 1. Comparison between the latex of the Burmese lacquer tree and the latex of the Japanese lacquer tree. Nogei Kagakukai-shi. 36:1962;527-531.
    • (1962) Nogei Kagakukai-shi , vol.36 , pp. 527-531
    • Oda, Y.1    Ishida, T.2    Honnda, K.3
  • 155
    • 0002722913 scopus 로고
    • Structural studies of plant gum from sap of the lac tree, Rhus vermicifera
    • Oshima R., Kumanotani J. Structural studies of plant gum from sap of the lac tree, Rhus vermicifera. Carbohydr Res. 127:1984;43-57.
    • (1984) Carbohydr Res , vol.127 , pp. 43-57
    • Oshima, R.1    Kumanotani, J.2
  • 156
    • 85013718794 scopus 로고    scopus 로고
    • Structural analysis of polysaccharides in Chinese lacquer by NMR spectroscopy
    • Lu R., Yoshida T., Uryu T. Structural analysis of polysaccharides in Chinese lacquer by NMR spectroscopy. Sen'i Gakkai-shi. 55:1999;47-56.
    • (1999) Sen'i Gakkai-shi , vol.55 , pp. 47-56
    • Lu, R.1    Yoshida, T.2    Uryu, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.