✦ LIBER ✦

N-Glycosyl Amides: Removal of the Anomeric Protecting Group and Conversion into Glycosyl Donors.

✍ Scribed by Norbert Pleuss; Horst Kunz

Publisher: John Wiley and Sons
Year: 2003
Weight: 159 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200344186

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

N-Glycosyl Amides: Removal of the Anomer

N-Glycosyl Amides: Removal of the Anomeric Protecting Group and Conversion into Glycosyl Donors

✍ Norbert Pleuss; Horst Kunz 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 112 KB 👁 2 views

MMTr as an Efficient Anomeric S-Protecti

MMTr as an Efficient Anomeric S-Protecting Group for the Synthesis of Glycosyl Thiols.

✍ Xiangming Zhu 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

Conversion of N-Acetylneuraminic Acid Gl

Conversion of N-Acetylneuraminic Acid Glycosyl Chloride into Dibenzyl Glycosyl Phosphate: O-Glycosylation in the Absence of a Promoter.

✍ A. M. Shpirt; L. O. Kononov; V. I. Torgov; V. N. Shibaev 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 118 KB

6-O-Silyl-N-acetyl-2-amino-2-N,3-O-carbo

6-O-Silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: Effective Glycosyl Acceptors in the Glucosamine 4-OH Series. Effect of Anomeric Stereochemistry on the Removal of the Oxazolidinone Group.

✍ David Crich; A. U. Vinod 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 42 KB 👁 2 views

N-Nosyl as a Stereoselectivity-Improving

N-Nosyl as a Stereoselectivity-Improving and Easily Removable Group in the O-Glycosylation of D-Allal and D-Galactal-Derived Allyl Aziridines. Stereospecific Synthesis of 4-Amino-2,3-unsaturated-O-glycosides.

✍ Valeria Di Bussolo; Maria Rosaria Romano; Mauro Pineschi; Paolo Crotti 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

## 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.

ChemInform Abstract: Why Are the Hydroxy

ChemInform Abstract: Why Are the Hydroxy Groups of Partially Protected N-Acetylglucosamine Derivatives Such Poor Glycosyl Acceptors, and What Can Be Done about It? A Comparative Study of the Reactivity of N-Acetyl-, N-Phthalimido-, and 2-azido-2-deoxy-glucosamine Derivatives in Glycosylation. 2-Picolinyl Ethers as Reactivity-Enhancing Replacements for Benzyl Ethers.

✍ David Crich; Vadim Dudkin 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views