메뉴 건너뛰기




Volumn , Issue 6, 1999, Pages 737-740

Bis C-glycosylated diphenylmethanes for stable glycoepitope mimetics

Author keywords

Additive; Aryl C glycoside; Mimetic; Sialyl Lewis X; Stifle coupling reaction

Indexed keywords

DIPHENYLMETHANE DERIVATIVE; GLYCOSIDE; UNCLASSIFIED DRUG;

EID: 0033067759     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2738     Document Type: Article
Times cited : (6)

References (24)
  • 3
    • 0028577585 scopus 로고
    • Parker, K. A.; Koh, Y-H. J. Am. Chem. Soc. 1994, 116, 11149. Johnson, C. R.; Johns, B. A. Synlett 1997, 1406. Kuribayashi, T.; Ohkawa, N.; Satoh, S. Tetrahedron Lett. 1998, 39, 4541.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 11149
    • Parker, K.A.1    Koh, Y.-H.2
  • 4
    • 0002412759 scopus 로고    scopus 로고
    • Parker, K. A.; Koh, Y-H. J. Am. Chem. Soc. 1994, 116, 11149. Johnson, C. R.; Johns, B. A. Synlett 1997, 1406. Kuribayashi, T.; Ohkawa, N.; Satoh, S. Tetrahedron Lett. 1998, 39, 4541.
    • (1997) Synlett , pp. 1406
    • Johnson, C.R.1    Johns, B.A.2
  • 5
    • 0032543463 scopus 로고    scopus 로고
    • Parker, K. A.; Koh, Y-H. J. Am. Chem. Soc. 1994, 116, 11149. Johnson, C. R.; Johns, B. A. Synlett 1997, 1406. Kuribayashi, T.; Ohkawa, N.; Satoh, S. Tetrahedron Lett. 1998, 39, 4541.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4541
    • Kuribayashi, T.1    Ohkawa, N.2    Satoh, S.3
  • 6
    • 0000103227 scopus 로고
    • Stille, J. K. Angew. Chem. 1986, 98, 504; Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Mitchell, T. N. Synthesis 1992, 803. Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis; Wiley: New York, 1995. Farina, V.; Krishnamurthy, V.; Scott, W. J. Organic Reactions, Vol. 50; Paquette, L. A., Ed.; Wiley: New York, 1997; p 1.
    • (1986) Angew. Chem. , vol.98 , pp. 504
    • Stille, J.K.1
  • 7
    • 84985570392 scopus 로고
    • Stille, J. K. Angew. Chem. 1986, 98, 504; Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Mitchell, T. N. Synthesis 1992, 803. Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis; Wiley: New York, 1995. Farina, V.; Krishnamurthy, V.; Scott, W. J. Organic Reactions, Vol. 50; Paquette, L. A., Ed.; Wiley: New York, 1997; p 1.
    • (1986) Angew. Chem. Int. Ed. Engl. , vol.25 , pp. 508
  • 8
    • 0026699017 scopus 로고
    • Stille, J. K. Angew. Chem. 1986, 98, 504; Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Mitchell, T. N. Synthesis 1992, 803. Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis; Wiley: New York, 1995. Farina, V.; Krishnamurthy, V.; Scott, W. J. Organic Reactions, Vol. 50; Paquette, L. A., Ed.; Wiley: New York, 1997; p 1.
    • (1992) Synthesis , pp. 803
    • Mitchell, T.N.1
  • 9
    • 0003441482 scopus 로고
    • Wiley: New York
    • Stille, J. K. Angew. Chem. 1986, 98, 504; Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Mitchell, T. N. Synthesis 1992, 803. Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis; Wiley: New York, 1995. Farina, V.; Krishnamurthy, V.; Scott, W. J. Organic Reactions, Vol. 50; Paquette, L. A., Ed.; Wiley: New York, 1997; p 1.
    • (1995) Palladium Reagents and Catalysts: Innovations in Organic Synthesis
    • Tsuji, J.1
  • 10
    • 0000802361 scopus 로고    scopus 로고
    • Paquette, L. A., Ed.; Wiley: New York
    • Stille, J. K. Angew. Chem. 1986, 98, 504; Angew. Chem. Int. Ed. Engl. 1986, 25, 508. Mitchell, T. N. Synthesis 1992, 803. Tsuji, J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis; Wiley: New York, 1995. Farina, V.; Krishnamurthy, V.; Scott, W. J. Organic Reactions, Vol. 50; Paquette, L. A., Ed.; Wiley: New York, 1997; p 1.
    • (1997) Organic Reactions , vol.50 , pp. 1
    • Farina, V.1    Krishnamurthy, V.2    Scott, W.J.3
  • 14
    • 0025176058 scopus 로고
    • Destannylation of electron-rich arylstannane, see: Tius, M. A.; Gu, X-q.; Gomez-Galeno, J. J. Am. Chem. Soc. 1990, 112, 8188. Keay, B. A.; Bontront, J-L, J. Can. J. Chem. 1991, 69, 1326. Saá, J. M.; Martorell, G. J. Org. Chem. 1993, 58, 1963.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 8188
    • Tius, M.A.1    Gu, X-q.2    Gomez-Galeno, J.3
  • 15
    • 0025176058 scopus 로고
    • Destannylation of electron-rich arylstannane, see: Tius, M. A.; Gu, X-q.; Gomez-Galeno, J. J. Am. Chem. Soc. 1990, 112, 8188. Keay, B. A.; Bontront, J-L, J. Can. J. Chem. 1991, 69, 1326. Saá, J. M.; Martorell, G. J. Org. Chem. 1993, 58, 1963.
    • (1991) Can. J. Chem. , vol.69 , pp. 1326
    • Keay, B.A.1    Bontront, J.-L.J.2
  • 16
    • 0000557056 scopus 로고
    • Destannylation of electron-rich arylstannane, see: Tius, M. A.; Gu, X-q.; Gomez-Galeno, J. J. Am. Chem. Soc. 1990, 112, 8188. Keay, B. A.; Bontront, J-L, J. Can. J. Chem. 1991, 69, 1326. Saá, J. M.; Martorell, G. J. Org. Chem. 1993, 58, 1963.
    • (1993) J. Org. Chem. , vol.58 , pp. 1963
    • Saá, J.M.1    Martorell, G.2
  • 17
    • 0027742959 scopus 로고
    • Brandley, B. K.; Kiso, M.; Abbas, S.; Nikrad, P.; Srivasatava, O.; Foxall, C.; Oda, Y.; Hasegawa, A. Glycobiology 1993, 6, 633. Ramphal, J. Y.; Zheng, Z-L.; Perez, C.; Walker, L. E.; DeFrees, S. A.; Gaeta, F. C. A. J. Med. Chem. 1994, 37, 3459. Kogan, T. P.; DuprÈ, B.; Keller, K. M.; Scott, I. L.; Bui, H.; Market, R. V.; Beck, P. J.; Voytus, J. A.; Revelle, B. M.; Scott, D. J. Med. Chem. 1995, 38, 4976.
    • (1993) Glycobiology , vol.6 , pp. 633
    • Brandley, B.K.1    Kiso, M.2    Abbas, S.3    Nikrad, P.4    Srivasatava, O.5    Foxall, C.6    Oda, Y.7    Hasegawa, A.8
  • 18
    • 0028073585 scopus 로고
    • Brandley, B. K.; Kiso, M.; Abbas, S.; Nikrad, P.; Srivasatava, O.; Foxall, C.; Oda, Y.; Hasegawa, A. Glycobiology 1993, 6, 633. Ramphal, J. Y.; Zheng, Z-L.; Perez, C.; Walker, L. E.; DeFrees, S. A.; Gaeta, F. C. A. J. Med. Chem. 1994, 37, 3459. Kogan, T. P.; DuprÈ, B.; Keller, K. M.; Scott, I. L.; Bui, H.; Market, R. V.; Beck, P. J.; Voytus, J. A.; Revelle, B. M.; Scott, D. J. Med. Chem. 1995, 38, 4976.
    • (1994) J. Med. Chem. , vol.37 , pp. 3459
    • Ramphal, J.Y.1    Zheng, Z.-L.2    Perez, C.3    Walker, L.E.4    DeFrees, S.A.5    Gaeta, F.C.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.