Glycosidation of 3,4,6-tri-o-benzyl-2-ethenyl-D-glucal - A route to 2-C-(β-methyl)methylene glycosides

Journal of Carbohydrate Chemistry

Volumn 19, Issue 6, 2000, Pages 661-675

  Feit, Ben Ami ^b   Kelson, Idil Kasuto ^b   Gerull, Anke ^a   Abramson, Sarah ^b   Schmidt, Richard R ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0034407891     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328300008544109     Document Type: Article

References (32)

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31. The ROESY (600 MHz) spectrum was measured at 1.0-6.0 ppm, and only the interactions, necessary for establishing the structures, are noted by the arrows. The anomeric configuration of the glycosyl donor (a) and the stereochemistry of the double bond (Z) was established based on the ROESY spectrum.
32. The ROESY (600 MHz) spectrum was measured at 1.1-6.0 ppm, and most of the important interactions, necessary for establishing the structures, are noted by the arrows. The anomeric configuration of the glycosyl donor (α) and the stereochemistry of the double bond (Z) was established based on the ROESY spectrum.