Synthesis of sucrose carbonates in aqueous medium

Journal of the Chemical Society - Perkin Transactions 1

Volumn , Issue 7, 1998, Pages 1179-1181

  Wernicke, Angelika ^a   Belniak, Stanislaw ^a   Thévenet, Sophie ^a   Descotes, Gérard ^a   Bouchu, Alain ^a   Queneau, Yves ^a  

^a Beghin Say UMR 143   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33748845958     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a800096d     Document Type: Article

References (14)

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4. P. J. Kocienski, Protecting Groups, Georg Thieme Verlag, Stuttgart, 1994.
5. -1, RI detection.
6. 2-allyl), 63.0, 62.7, 62.3, 61.8, 61.0, 60,7 (non-carbonated C-6, 1′, 6′).
7. A. Lubineau, J. Augé, H. Bienaymé, Y. Queneau and M.-C. Scherrmann, in Carbohydrates as Organic Raw Materials II, ed. G. Descotes, VCH, Weinheim, 1993, p. 99;
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12. The polysubstituted sucrose octylcarbonates, when formed rapidly, tend to separate out of the reaction mixture, and often cover the glassware as well as the pH-stat electrode, preventing an accurate measure and control of the basic conditions.
13. 3) 516.
14. A. Lubineau, G. Bouchain and Y. Queneau, J. Chem. Soc., Perkin Trans. 1, 1995, 2433.