Trityl salt catalyzed stereoselective glycosylation of alcohols with 1-hydroxyribofuranose

Chemistry Letters

Volumn , Issue 1, 1996, Pages 79-80

  Uchiro, Hiromi ^a   Mukaiyama, Temaki ^a  

^a TOKYO UNIVERSITY OF SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0030552065     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1996.79     Document Type: Article

References (12)

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3. P. Sinaÿ, Pure and Appl. Chem., 63, 519 (1991), and references cited therein.
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8. T. Mukaiyama, K. Matsubara, and M. Hora, Synthesis, 1994, 1368.
9. We already reported that equimolar or catalytic amount of trityl perchlorate was effectively employed in the reactions of 1-O-acylsugars with alcohols or silyl nucleophiles to afford the corresponding O- and C-glycosides in good yields with high stereoselectivities, a) T. Mukaiyama, S. Kobayashi, and S. Shoda, Chem. Lett., 1984, 907;
10. b) T. Mukaiyama, S. Kobayashi, and S. Shoda, Chem. Lett., 1984, 1529.
11. T. Yamanoi and T. Inazu, Chem. Lett., 1990, 849.
12. J. C. W. Chien, W.-M. Tsai, M. D. Rausch, J. Am. Chem. Soc., 113, 8570 (1991).