共 12 条
[1]
BELBAULT GM, 1972, CAN J CHEM, V50, P3373
[2]
THE ALLYL GROUP FOR PROTECTION IN CARBOHYDRATE-CHEMISTRY .14. SYNTHESIS OF 2,3-DI-O-METHYL-4-O-(3,6-DI-O-METHYL-BETA-D-GLUCOPYRANOSYL)-L-RHAMNOPYRANOSE (AND ITS ALPHA-PROPYL GLYCOSIDE) - A HAPTENIC PORTION OF THE MAJOR GLYCOLIPID FROM MYCOBACTERIUM-LEPRAE
[J].
JOURNAL OF CARBOHYDRATE CHEMISTRY,
1983, 2 (03)
:207-223
[3]
KLEMER A, 1983, LIEBIGS ANN CHEM, P1416
[5]
PITT TL, 1984, METHOD MICROBIOL, V15, P173
[6]
POZSGAY V, 1980, CARBOHYD RES, V86, P143
[7]
NEW METHODS FOR THE SYNTHESIS OF GLYCOSIDES AND OLIGOSACCHARIDES - ARE THERE ALTERNATIVES TO THE KOENIGS-KNORR METHOD
[J].
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH,
1986, 25 (03)
:212-235
[9]
SYNTHESIS OF 4 SPACER-CONTAINING TRISACCHARIDES WITH THE 4-O-(BETA-L-RHAMNOPYRANOSYL)-D-GLUCOPYRANOSE UNIT IN COMMON, REPRESENTING FRAGMENTS OF CAPSULAR POLYSACCHARIDES FROM STREPTOCOCCUS-PNEUMONIAE TYPE-2, TYPE-7F, TYPE-22F, AND TYPE-23F
[J].
JOURNAL OF CARBOHYDRATE CHEMISTRY,
1992, 11 (06)
:665-689
[10]
WARREN CD, 1977, CARBOHYD RES, V53, P67