1996
DOI: 10.1016/s0008-6215(96)90184-6
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Synthesis of O- and S-glucosides using glucosyl halides and zinc salts

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Cited by 7 publications
(3 citation statements)
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“…We also investigated various “nonheavy” metal salts as promoters, with or without I 2 present. The use of Zn halides with a glucuronyl bromide but with no added I 2 had been reported previously, and a few other metal salts have been used in conjunction with glucosyl bromides . The results for the model reaction, Scheme , are summarized in Table .…”
mentioning
confidence: 91%
“…We also investigated various “nonheavy” metal salts as promoters, with or without I 2 present. The use of Zn halides with a glucuronyl bromide but with no added I 2 had been reported previously, and a few other metal salts have been used in conjunction with glucosyl bromides . The results for the model reaction, Scheme , are summarized in Table .…”
mentioning
confidence: 91%
“…Similarly, compounds 9 and 10 were converted to diglycosides (11, 13, 15) by method A, and to monoglycosides (12,14,16) by method B (Table 1).…”
Section: Synthesis Of Glycosylcurcuminoidsmentioning
confidence: 99%
“…mp 142°C 16) was dried under reduced pressure at 250°C for 3 h. The dried oxide (0.13 g, 1.8 mmol) was added to acetylacetone (0.25 g, 2.5 mmol) and the mixture was stirred at room temperature for 30 min, and then used directly.…”
mentioning
confidence: 99%