메뉴 건너뛰기




Volumn 37, Issue 17, 1998, Pages 2373-2376

Synthesis of hyperbranched aminopolysaccharides

Author keywords

Carbohydrates; Dendrimers; Glycosylations

Indexed keywords


EID: 0032544631     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-3773(19980918)37:17<2373::aid-anie2373>3.0.co;2-b     Document Type: Article
Times cited : (43)

References (35)
  • 2
    • 0025373701 scopus 로고
    • a) D. A. Tomalia, A. M. Naylor, W. A. Goddard III, Angew. Chem. 1990, 102, 119; Angew. Chem. Int. Ed. Engl. 1990, 29, 138;
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 138
  • 11
    • 0027740240 scopus 로고
    • For example, a) R. Roy, D. Zanini, S. J. Meunier, A. Romanowska, J. Chem. Soc. Chem. Commun. 1993, 1869; b) K. Aoi, K. Itoh, M. Okada, Macromolecules 1995, 28, 5391; c) P. R. Ashton, S. E. Boyd, C. L. Brown, N. Jayaramen, S. A. Nepogodiev, J. F. Stoddart, Chem. Eur. J. 1996, 2, 1115; d) D. Zanini, R. Roy, J. Org. Chem. 1996, 61, 7348; e) D. Zanini, R. Roy, J. Am. Chem. Soc. 1997, 119, 2088.
    • (1993) J. Chem. Soc. Chem. Commun. , pp. 1869
    • Roy, R.1    Zanini, D.2    Meunier, S.J.3    Romanowska, A.4
  • 12
    • 0001002781 scopus 로고
    • For example, a) R. Roy, D. Zanini, S. J. Meunier, A. Romanowska, J. Chem. Soc. Chem. Commun. 1993, 1869; b) K. Aoi, K. Itoh, M. Okada, Macromolecules 1995, 28, 5391; c) P. R. Ashton, S. E. Boyd, C. L. Brown, N. Jayaramen, S. A. Nepogodiev, J. F. Stoddart, Chem. Eur. J. 1996, 2, 1115; d) D. Zanini, R. Roy, J. Org. Chem. 1996, 61, 7348; e) D. Zanini, R. Roy, J. Am. Chem. Soc. 1997, 119, 2088.
    • (1995) Macromolecules , vol.28 , pp. 5391
    • Aoi, K.1    Itoh, K.2    Okada, M.3
  • 13
    • 28444476615 scopus 로고    scopus 로고
    • For example, a) R. Roy, D. Zanini, S. J. Meunier, A. Romanowska, J. Chem. Soc. Chem. Commun. 1993, 1869; b) K. Aoi, K. Itoh, M. Okada, Macromolecules 1995, 28, 5391; c) P. R. Ashton, S. E. Boyd, C. L. Brown, N. Jayaramen, S. A. Nepogodiev, J. F. Stoddart, Chem. Eur. J. 1996, 2, 1115; d) D. Zanini, R. Roy, J. Org. Chem. 1996, 61, 7348; e) D. Zanini, R. Roy, J. Am. Chem. Soc. 1997, 119, 2088.
    • (1996) Chem. Eur. J. , vol.2 , pp. 1115
    • Ashton, P.R.1    Boyd, S.E.2    Brown, C.L.3    Jayaramen, N.4    Nepogodiev, S.A.5    Stoddart, J.F.6
  • 14
    • 0000439588 scopus 로고    scopus 로고
    • For example, a) R. Roy, D. Zanini, S. J. Meunier, A. Romanowska, J. Chem. Soc. Chem. Commun. 1993, 1869; b) K. Aoi, K. Itoh, M. Okada, Macromolecules 1995, 28, 5391; c) P. R. Ashton, S. E. Boyd, C. L. Brown, N. Jayaramen, S. A. Nepogodiev, J. F. Stoddart, Chem. Eur. J. 1996, 2, 1115; d) D. Zanini, R. Roy, J. Org. Chem. 1996, 61, 7348; e) D. Zanini, R. Roy, J. Am. Chem. Soc. 1997, 119, 2088.
    • (1996) J. Org. Chem. , vol.61 , pp. 7348
    • Zanini, D.1    Roy, R.2
  • 15
    • 0030971899 scopus 로고    scopus 로고
    • For example, a) R. Roy, D. Zanini, S. J. Meunier, A. Romanowska, J. Chem. Soc. Chem. Commun. 1993, 1869; b) K. Aoi, K. Itoh, M. Okada, Macromolecules 1995, 28, 5391; c) P. R. Ashton, S. E. Boyd, C. L. Brown, N. Jayaramen, S. A. Nepogodiev, J. F. Stoddart, Chem. Eur. J. 1996, 2, 1115; d) D. Zanini, R. Roy, J. Org. Chem. 1996, 61, 7348; e) D. Zanini, R. Roy, J. Am. Chem. Soc. 1997, 119, 2088.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2088
    • Zanini, D.1    Roy, R.2
  • 26
    • 0025699247 scopus 로고
    • S. Nishimura, K. Matsuoka, K. Kurita, Macromolecules 1990, 23, 4182. It has been reported that 10-camphorsulfonic acid is a more effective catalyst than, for example, p-toluenesulfonic acid and trifluoromethanesulfonic acid in glycosylations with a dihydrooxazole glycosyl donor.
    • (1990) Macromolecules , vol.23 , pp. 4182
    • Nishimura, S.1    Matsuoka, K.2    Kurita, K.3
  • 27
    • 0344710478 scopus 로고    scopus 로고
    • note
    • Nucleophilic attack of a nitrogen atom in the dihydrooxazole group of 1 onto p-toluenesulfonate group at position 6 could take place during the polymerization. However, an acetyl-protected derivative of 1 was stable when heated under reflux in 1,2-dichloroethane, which indicates no reaction had occurred between the dihydrooxazole and p-toluenesulfonate groups.
  • 28
    • 85087234552 scopus 로고    scopus 로고
    • note
    • 4), 168.4-171.4 (C=O).
  • 34
    • 85087235796 scopus 로고    scopus 로고
    • note
    • 2 was observed by TLC, and 75.6% of 5 was recovered from the reaction mixture as a hexane-insoluble fraction.
  • 35
    • 0345572478 scopus 로고    scopus 로고
    • note
    • [17]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.