𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Trityl ethers in oligosaccharide synthesis: A novel strategy for the convergent assembly of oligosaccharides

✍ Scribed by Geert-Jan Boons; Simeon Bowers; Diane M. Coe


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
248 KB
Volume
38
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


We have developed a novel glycosylation strategy in which a tritylated thioglycoside can act as a glycosyl donor and acceptor. In combination with previously reported chemoselective glyeosylations, this feature enables highly convergent assembly of ofigosacchaddes


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Trityl Ethers in Ol
✍ G.-J. BOONS; S. BOWERS; D. M. COE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 27 KB πŸ‘ 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 β€œFull Text” option. The original article is trackable v

A two directional glycosylation strategy
✍ Tong Zhu; Geert-Jan Boons πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 239 KB

A novel glycosylation strategy has been developed whereby a silyl protected thioglycoside can act as both glycosyl donor and acceptor. Taking advantage of a two directional approach in combination with previously reported orthogonal glycosylations, enables highly convergent and versatile assembly of

ChemInform Abstract: Novel Regioselectiv
✍ G.-J. BOONS; T. ZHU πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 26 KB πŸ‘ 1 views

Novel Regioselective Glycosylations for the Convergent and Chemoselective Assembly of Oligosaccharides. -The novel chemoselective glycosylation strategy, which is based on the differences in reactivity between hydroxyl groups of a glycosyl donor such as (I) and an acceptor, e.g. (II), provides a pr