DI-TOSYLIERUNG DER GLUCOSE

[1] Conversion of 2-p-toluenesulphonyl beta-methylglucoside into methyl epi glucosamme [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1934, : 151 - 154

[2] The unimolar tosylation of alpha- and beta -methyl-d-glucosides [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 : 395 - 399

[3] *UBER DIE HERSTELLUNG VON ALPHA-CHINOVOSE-TETRAACETAT UND BETA-CHINOVOSE-TETRAACETAT AUS GLUCOSE [J]. HELVETICA CHIMICA ACTA, 1946, 29 (05) : 1199 - 1203

[4] *GLUCOSIDE UND BETA-1,3,4,6-TETRAACETYL-GLUCOSE AUS TRIACETYL-GLUCOSAN-ALPHA-[1,2]BETA[1,5] [J]. HELVETICA CHIMICA ACTA, 1948, 31 (01) : 281 - 286

[5] The anhydromethylhexoside formed by the alkaline hydrolysis of 2-p-toluenesulphonyl triacetyl beta-methylglucoside. Characterisation of 2 : 4 : 6-trimethyl glucose. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1938, : 1417 - 1421

[6] McIlwain H, 1941, BIOCHEM J, V35, P1311

[7] REYNOLDS TM, 1933, J CHEM SOC, P224

[8] REYNOLDS TM, 1931, J CHEM SOC, P2626

[9] RYBAK B, IN PRESS EXPERIENTIA

[1] Conversion of 2-p-toluenesulphonyl beta-methylglucoside into methyl epi glucosamme [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1934, : 151 - 154

[2] The unimolar tosylation of alpha- and beta -methyl-d-glucosides [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 : 395 - 399

[3] *UBER DIE HERSTELLUNG VON ALPHA-CHINOVOSE-TETRAACETAT UND BETA-CHINOVOSE-TETRAACETAT AUS GLUCOSE [J]. HELVETICA CHIMICA ACTA, 1946, 29 (05) : 1199 - 1203

[4] *GLUCOSIDE UND BETA-1,3,4,6-TETRAACETYL-GLUCOSE AUS TRIACETYL-GLUCOSAN-ALPHA-[1,2]BETA[1,5] [J]. HELVETICA CHIMICA ACTA, 1948, 31 (01) : 281 - 286

[5] The anhydromethylhexoside formed by the alkaline hydrolysis of 2-p-toluenesulphonyl triacetyl beta-methylglucoside. Characterisation of 2 : 4 : 6-trimethyl glucose. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1938, : 1417 - 1421

[6] McIlwain H, 1941, BIOCHEM J, V35, P1311

[7] REYNOLDS TM, 1933, J CHEM SOC, P224

[8] REYNOLDS TM, 1931, J CHEM SOC, P2626

[9] RYBAK B, IN PRESS EXPERIENTIA