SYNTHESIS OF 6-O-(ALPHA-D-MANNOPYRANOSYL)-D-MYO-INOSITOL - A FRAGMENT FROM MYCOBACTERIA PHOSPHOLIPIDS

被引:54
作者
ELIE, CJJ [1 ]
VERDUYN, R [1 ]
DREEF, CE [1 ]
BROUNTS, DM [1 ]
VANDERMAREL, GA [1 ]
VANBOOM, JH [1 ]
机构
[1] GORLAEUS LABS,POB 9502,2300 RA LEIDEN,NETHERLANDS
关键词
D O I
10.1016/S0040-4020(01)81480-0
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Condensation of 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl fluoride (12) or ethyl 2-O- benzoyl-3,4,6-tri-0-benzyl-1-thio-α-D-mannopyranoside (13) with racemic 1,2-0-cyclohexylidene-3,4,5 tri-O-benzyl- myo-inositol (11) gave, after deacylation and column chromatography, the enantiomorphs 16a and 16b. Benzylation, acid hydrolysis of the 1,2-O-cyclohexylidene group and regioselective allylation of 16b led to 4b, which was deblocked by deallylation and hydrogenolysis to give 6-O-(α-O-D-mannopyranosyl)-D-myo-inositol (5b). Any attempt to glycosylate the hydroxyl at the axial C-2 position of the myo-inositol moiety in 4b with the mannopyranosyl fluoride 12 or the ethyl thiomannopyranoside 13 failed. © 1990.
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页码:8243 / 8254
页数:12
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