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Volumn 17, Issue 4-5, 1998, Pages 609-631

Scope and applications of "active and latent" thioglycosyl donors. Part 4

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[No Author keywords available]

Indexed keywords


EID: 0043218397     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328309808002341     Document Type: Article
Times cited : (37)

References (26)
  • 1
    • 0346956053 scopus 로고    scopus 로고
    • note
    • Dedicated to the memory of Professor Akira Hasegawa.
  • 2
    • 0026675928 scopus 로고
    • For part 1-3, see, respectively: (a) R. Roy, F. O. Andersson and M. Letellier, Tetrahedron Lett., 33, 6053 (1992); (b) S. Cao, S. J. Meunier, F. O. Andersson, M. Letellier and R. Roy, Tetrahedron: Asymmetry, 5, 2303 (1994); S. Cao and R. Roy, Tetrahedron Lett., 37, 3421 (1996).
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6053
    • Roy, R.1    Andersson, F.O.2    Letellier, M.3
  • 3
    • 0028004561 scopus 로고
    • For part 1-3, see, respectively: (a) R. Roy, F. O. Andersson and M. Letellier, Tetrahedron Lett., 33, 6053 (1992); (b) S. Cao, S. J. Meunier, F. O. Andersson, M. Letellier and R. Roy, Tetrahedron: Asymmetry, 5, 2303 (1994); S. Cao and R. Roy, Tetrahedron Lett., 37, 3421 (1996).
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 2303
    • Cao, S.1    Meunier, S.J.2    Andersson, F.O.3    Letellier, M.4    Roy, R.5
  • 4
    • 0029931703 scopus 로고    scopus 로고
    • For part 1-3, see, respectively: (a) R. Roy, F. O. Andersson and M. Letellier, Tetrahedron Lett., 33, 6053 (1992); (b) S. Cao, S. J. Meunier, F. O. Andersson, M. Letellier and R. Roy, Tetrahedron: Asymmetry, 5, 2303 (1994); S. Cao and R. Roy, Tetrahedron Lett., 37, 3421 (1996).
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3421
    • Cao, S.1    Roy, R.2
  • 5
    • 0348216854 scopus 로고    scopus 로고
    • note
    • Visiting Professor from Instituto de Biotecnologia, Facultad de Ciencias, Universidad de Granada, Granada, Spain.
  • 6
    • 0348216853 scopus 로고
    • Abstract No. CARB-92, Toronto, Canada, June 5-10
    • Previous accounts on thioglycosyl donors and their relative reactivity were initially described using mainly methyl triflate as the promotor: (a) B. A. Silwanis, F. Dasgupta and P. J. Garegg, Abstract No. CARB-92, 3rd Chemical Congress of North America, Toronto, Canada, June 5-10, 1988; (b) F. Dasgupta and P. J. Garegg, Carbohydr. Res., 202, 225 (1990); P. Fügedi, P. J. Garegg, S. Oscarson, G. Rosén and B. A. Silvanis, Carbohydr. Res., 211, 157 (1991); V. Pozsgay in Carbohydrates, Synthetic Methods and Applications in Medicinal Chemistry; H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan, 1992, p 188.
    • (1988) 3rd Chemical Congress of North America
    • Silwanis, B.A.1    Dasgupta, F.2    Garegg, P.J.3
  • 7
    • 0025708123 scopus 로고
    • Previous accounts on thioglycosyl donors and their relative reactivity were initially described using mainly methyl triflate as the promotor: (a) B. A. Silwanis, F. Dasgupta and P. J. Garegg, Abstract No. CARB-92, 3rd Chemical Congress of North America, Toronto, Canada, June 5-10, 1988; (b) F. Dasgupta and P. J. Garegg, Carbohydr. Res., 202, 225 (1990); P. Fügedi, P. J. Garegg, S. Oscarson, G. Rosén and B. A. Silvanis, Carbohydr. Res., 211, 157 (1991); V. Pozsgay in Carbohydrates, Synthetic Methods and Applications in Medicinal Chemistry; H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan, 1992, p 188.
    • (1990) Carbohydr. Res. , vol.202 , pp. 225
    • Dasgupta, F.1    Garegg, P.J.2
  • 8
    • 0026413082 scopus 로고
    • Previous accounts on thioglycosyl donors and their relative reactivity were initially described using mainly methyl triflate as the promotor: (a) B. A. Silwanis, F. Dasgupta and P. J. Garegg, Abstract No. CARB-92, 3rd Chemical Congress of North America, Toronto, Canada, June 5-10, 1988; (b) F. Dasgupta and P. J. Garegg, Carbohydr. Res., 202, 225 (1990); P. Fügedi, P. J. Garegg, S. Oscarson, G. Rosén and B. A. Silvanis, Carbohydr. Res., 211, 157 (1991); V. Pozsgay in Carbohydrates, Synthetic Methods and Applications in Medicinal Chemistry; H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan, 1992, p 188.
    • (1991) Carbohydr. Res. , vol.211 , pp. 157
    • Fügedi, P.1    Garegg, P.J.2    Oscarson, S.3    Rosén, G.4    Silvanis, B.A.5
  • 9
    • 0004128113 scopus 로고
    • H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan
    • Previous accounts on thioglycosyl donors and their relative reactivity were initially described using mainly methyl triflate as the promotor: (a) B. A. Silwanis, F. Dasgupta and P. J. Garegg, Abstract No. CARB-92, 3rd Chemical Congress of North America, Toronto, Canada, June 5-10, 1988; (b) F. Dasgupta and P. J. Garegg, Carbohydr. Res., 202, 225 (1990); P. Fügedi, P. J. Garegg, S. Oscarson, G. Rosén and B. A. Silvanis, Carbohydr. Res., 211, 157 (1991); V. Pozsgay in Carbohydrates, Synthetic Methods and Applications in Medicinal Chemistry; H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan, 1992, p 188.
    • (1992) Carbohydrates, Synthetic Methods and Applications in Medicinal Chemistry , pp. 188
    • Pozsgay, V.1
  • 17
    • 0004111999 scopus 로고    scopus 로고
    • S. H. Khan and R. A. O'Neil, Eds; Harwood Academic Publishers: Amsterdam, Netherlands
    • (b) T. Norberg in Modern Methods in Carbohydrate Chemistry; S. H. Khan and R. A. O'Neil, Eds; Harwood Academic Publishers: Amsterdam, Netherlands, 1996, p 82;
    • (1996) Modern Methods in Carbohydrate Chemistry , pp. 82
    • Norberg, T.1


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