✦ LIBER ✦

A novel method for synthesis of chitobiose via enzymatic glycosylation using a sugar oxazoline as glycosyl donor

✍ Scribed by Shiro Kobayashi; Toshitsugu Kiyosada; Shin-ichiro Shoda

Publisher: Elsevier Science
Year: 1997
Tongue: French
Weight: 123 KB
Volume: 38
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(97)00319-5

No coin nor oath required. For personal study only.

✦ Synopsis

A convenient method for synthesis of N,N'-diacetylchitobiose, an important building block for oligo and polysaccharide synthesis, has been developed by using a 1,2-oxagoline derivative of Nacetylglucosamine as new glycosyl donor for chitinase.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Novel Method for

ChemInform Abstract: A Novel Method for Synthesis of Chitobiose via Enzymatic Glycosylation Using a Sugar Oxazoline as Glycosyl Donor.

✍ S. KOBAYASHI; T. KIYOSADA; S. SHODA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Sulfurylchloride/trifluoromethanesulfoni

Sulfurylchloride/trifluoromethanesulfonic acid. A novel promoter system for glycoside synthesis using thioglycosides as glycosyl donors

✍ Hans Lönn 📂 Article 📅 1987 🏛 Springer US 🌐 English ⚖ 75 KB

ChemInform Abstract: Use of a Phenyl 1-S

ChemInform Abstract: Use of a Phenyl 1-Selenogalactofuranoside as a Glycosyl Donor for the Synthesis of Galactofuranosyl-Containing Disaccharides.

✍ Blair D. Johnston; B. Mario Pinto 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

A novel glycosyl donor for the synthesis

A novel glycosyl donor for the synthesis of cancer specific core 5 and sialyl core 5 as glycopeptide building blocks

✍ Dongxu Qiu; R.Rao Koganty 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 225 KB

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

ChemInform Abstract: A New, Efficient Gl

ChemInform Abstract: A New, Efficient Glycosylation Method for Oligosaccharide Synthesis under Neutral Conditions: Preparation and Use of New DISAL Donors.

✍ Lars Petersen; Knud J. Jensen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

## 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

The use of 2,6-anhydro-2-thio sugar for

The use of 2,6-anhydro-2-thio sugar for a highly stereocontrolled glycosylation: A novel strategy for synthesis of 2,6-dideoxy-α-glycosides

✍ Kazunobu Toshima; Satsuki Mukaiyama; Takashi Ishiyama; Kuniaki Tatsuta 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 258 KB

## Summarv: A novel and efficient synthesis of 2,6-dideoxy-a-glycosides was developed by use of phenyl 2,6-anhydro-1,2-dithio-D-altropyranosides as glycosyl donors in a highly stereocontrolled glycosyla tion . Highly stereocontrolled synthesis of 2,6-dideoxy glycosides is of considerable interest