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1990
DOI: 10.1016/0008-6215(90)84180-3
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An n.m.r. and conformational analysis of the terminal trisaccharide from the serologically active glycolipid of Mycobacterium leprae in different solvents

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Cited by 12 publications
(3 citation statements)
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“…The conformation of compounds 62 was also reported. 43 The (synthesized39 by Fujiwara) against sera from leprosy patients and control showed an obvious similarity: the presence of the innermost sugar did not contribute significantly to sensitivity or specificity. These di-and trisaccharide-containing artificial antigens were found to be suitable for the serodiagnosis of leprosy.…”
Section: -Di-o-acetyl-23-di-o-methyl-a-l-rhamnopyranose (58) By Usingmentioning
confidence: 95%
“…The conformation of compounds 62 was also reported. 43 The (synthesized39 by Fujiwara) against sera from leprosy patients and control showed an obvious similarity: the presence of the innermost sugar did not contribute significantly to sensitivity or specificity. These di-and trisaccharide-containing artificial antigens were found to be suitable for the serodiagnosis of leprosy.…”
Section: -Di-o-acetyl-23-di-o-methyl-a-l-rhamnopyranose (58) By Usingmentioning
confidence: 95%
“…Since the reported synthesis in 1988 multiple groups have synthesized one or multiple M. leprae PGL glycans [25,54–59] . Líptak and coworkers investigated a new approach towards PGL‐I in 1993 [59] .…”
Section: Leprae Pgl Glycansmentioning
confidence: 99%
“…[50][51][52][53] Since the reported synthesis in 1988 multiple groups have synthesized one or multiple M. leprae PGL glycans. [25,[54][55][56][57][58][59] Líptak and coworkers investigated a new approach towards PGL-I in 1993. [59] They set out to reduce the total amount of steps required by concurrently installing multiple methyl ethers in a single step (Scheme 3).…”
Section: R E C O R D R E V I E W T H E C H E M I C a L R E C O R Dmentioning
confidence: 99%