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0346956053
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note
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Dedicated to the memory of Professor Akira Hasegawa.
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0026675928
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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).
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Roy, R.1
Andersson, F.O.2
Letellier, M.3
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3
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0028004561
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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).
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Cao, S.1
Meunier, S.J.2
Andersson, F.O.3
Letellier, M.4
Roy, R.5
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4
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0029931703
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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).
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Cao, S.1
Roy, R.2
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5
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0348216854
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note
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Visiting Professor from Instituto de Biotecnologia, Facultad de Ciencias, Universidad de Granada, Granada, Spain.
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0348216853
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Abstract No. CARB-92, Toronto, Canada, June 5-10
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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.
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3rd Chemical Congress of North America
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Silwanis, B.A.1
Dasgupta, F.2
Garegg, P.J.3
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7
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0025708123
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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.
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Dasgupta, F.1
Garegg, P.J.2
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8
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0026413082
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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.
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Fügedi, P.1
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Silvanis, B.A.5
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9
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0004128113
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H. Ogura, A. Hasegawa and T. Suami, Eds.; VCH-Kodansha, Tokyo, Japan
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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.
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Pozsgay, V.1
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