## 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 “Full Text” option. The original article is trackable v
ChemInform Abstract: Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method.
✍ Scribed by D. CRICH; S. SUN
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Direct Synthesis of β-Mannopyranosides by the Sulfoxide Method.
-The activation of a glycosyl donor via the sulfoxide group followed by addition of a glycosyl acceptor in CH2Cl2 results in the formation of mannopyranosides in high yield and high β:α-ratios. Reducing the bulk of the O-2 protecting group leads to greater β:. alpha.-ratios for sec glycosyl acceptors. The very effective new method for the one-pot synthesis of the title compounds is generally applicable to a wide variety of prim and sec glycosyl acceptors. -(CRICH, D.;
📜 SIMILAR VOLUMES
Direct Chemical Synthesis of β-Mannopyranosides and Other Glycosides via Glycosyl Triflates. -New and efficient methods to prepare β-mannopyranosides like (III) and (VI) are reported. The use of a 4,6-O-benzylidene-protected mannose as well as non-participating protecting groups on O-2 and O-3 are
## 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 “Full Text” option. The original article is trackable v