𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Highly Stereoselective Synthesis of 1,2-trans-C-Glycosides via Glycosyl Samarium(III) Compounds

✍ Scribed by Daniel Mazéas; Dr. Troels Skrydstrup; Prof. Dr. Jean-Marie Beau

Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
456 KB
Volume
34
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Syn
ChemInform Abstract: Stereoselective Synthesis of α-C-(Alkynyl)-glycosides via Ring- Opening of α-1,2-Anhydrosugars.
✍ M. A. LEEUWENBURGH; C. M. TIMMERS; G. A. VAN DER MAREL; J. H. VAN BOOM; J.-M. MA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

Stereoselective Synthesis of α-C-(Alkynyl)-glycosides via Ring-Opening of α-1,2-Anhydrosugars. -In the presence of ZnCl2 the α-1,2-epoxide function in sugars is selectively ring-opened by lithium alkynyl derivatives to form α -glycosides with retention of configuration. -

Samarium Diiodide-Mediated Reductive Cou
Samarium Diiodide-Mediated Reductive Coupling of Epoxides and Carbonyl Compounds: A Stereocontrolled Synthesis of C-Glycosides from 1,2-Anhydro Sugars
✍ Jose Luis Chiara; Esther Sesmilo 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 105 KB 👁 2 views

adduct of 1 [tBu 4 PcInCl(tmed)], have been studied in toluene with laser pulses at 410 nm. These preliminary results show that 2 exhibits good optical-limiting response at this laser wavelength, whereas no response was found for compound 1 and its tmed adduct. Further studies on the NLO properties