1917
DOI: 10.1002/cber.191705001117
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Weitere Synthesen von Glucosiden mittels Acetobromglucose und Chinolin. Derivate von Menthol und Resorcin

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Cited by 25 publications
(2 citation statements)
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“…Materials. The following compounds were synthesized: phenyl a-D-glucopyranoside (Fischer & v. Mechel, 1916), phenyl ,-D-glucopyranoside (Fischer & Armstrong, 1901), (-)-menthyl a-D-glucopyranoside (Fischer & Bergmann, 1917), (-)-menthyl ,B-D -glucopyranoside (Treibs & Franke, 1950), methyl a-D-glucopyranoside (Helferich & Schiifer, 1948), methyl a-and ,-D-galactopyranosides (Dale & Hudson, 1930), methyl ac-D-mannopyranoside (Fischer, 1895), methyl ,-D-mannopyranoside i8opropanol solvate (Isbell & Frush, 1940).…”
Section: Methodsmentioning
confidence: 99%
“…Materials. The following compounds were synthesized: phenyl a-D-glucopyranoside (Fischer & v. Mechel, 1916), phenyl ,-D-glucopyranoside (Fischer & Armstrong, 1901), (-)-menthyl a-D-glucopyranoside (Fischer & Bergmann, 1917), (-)-menthyl ,B-D -glucopyranoside (Treibs & Franke, 1950), methyl a-D-glucopyranoside (Helferich & Schiifer, 1948), methyl a-and ,-D-galactopyranosides (Dale & Hudson, 1930), methyl ac-D-mannopyranoside (Fischer, 1895), methyl ,-D-mannopyranoside i8opropanol solvate (Isbell & Frush, 1940).…”
Section: Methodsmentioning
confidence: 99%
“…Borneol cC-D-glucopyranoside. The method was similar to that used to prepare menthyl a-D-glucopyranoside (Fischer & Bergmann, 1917). A mixture of borneol (optically inactive, 20 g.), tetra-O-acetyl-a-D-glucopyranosyl bromide (10 g.) and redistilled quinoline (5 g.) was heated on an oil bath at 105-110o for 2 hr.…”
Section: (A)mentioning
confidence: 99%