Application of tri-n-butyltin cuprate in sugar chemistry

Tetrahedron Letters

Volumn 37, Issue 17, 1996, Pages 3063-3066

  Jarosz, Sławomir ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARBOHYDRATE SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; TECHNIQUE;

EID: 0029947385     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00470-4     Document Type: Article

References (34)

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22. 2.
23. 4Cl, the organic phase was separated and the product was isolated by column chromatography (hexane - ethyl acetate, 6:1). Rection with sugar tosylate was carried out for 16 h at room temp.
24. 6.
25. 2.
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28. 13C-NMR δ: 135.1 (C-5), 118.8 (C-6), 81.7, 80.4, 79.5, 61.5 (C-1).
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34. 13C-NMR δ: 202.7 (CHO), 97.6 (C-1), 82.0 (C-3), 81.9 (C-4), 74.0 (C-5), 55.1 (OMe), 46.5 (C-6), 23.2 (C-7).