## Abstract For Abstract see ChemInform Abstract in Full Text.
A concise synthesis of the O-glycosylated amino acid building block; using phenyl selenoglycoside as a glycosyl donor
β Scribed by Weir-Torn Jiaang; Meng-Yang Chang; Ping-Hui Tseng; Shui-Tein Chen
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 126 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A new glycosylation methodology for synthesizing a protected TF antigen is described. The key step is to use phenyl selenoglycoside as a glycosyl donor, thereby successfully establishing O-linked Fmoc-protected threoninyl monosaccharide in an excellent yield with high Ξ± selectivity. From protected D-galactal, a protected TF antigen building block is obtained in 40% total yield.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Trichloroacetimidate at 1 and 3 position of 4.6-benzylidenyl N-acetylgalactosamine serves as a leaving group for glycosylation and a selective and acid sensitive protecting group respectively. This versatile donor, while forming exclusive a-glycoside with serine/threonine, serves as a fascile precur