𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Stereocontrolled Synthesis of 3′-Isomeric β-Nucleoside by Intramolecular Glycosylation.

✍ Scribed by K. SUJINO; H. SUGIMURA


Book ID
112021413
Publisher
John Wiley and Sons
Year
2010
Weight
28 KB
Volume
26
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: Stereocontrolled Sy
✍ X. XIA; J. WANG; M. W. HAGER; N. SISTI; D. C. LIOTTA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

Stereocontrolled Synthesis of β-2'-Deoxypyrimidine Nucleosides via Intramolecular Glycosylations. -In continuation of efforts to develop general methods for the exclusive formation of β-nucleosides, the base-promoted reaction of the pentafuranoside (II) with allyloxypyrimidines (II) is reported. Af

ChemInform Abstract: Stereocontrolled Sy
✍ Hideyuki Sugimura; Keiko Sujino 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 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

Stereocontrolled synthesis of β-2′-deoxy
✍ Xiaoyang Xia; Jianying Wang; Michael W. Hager; Nicholas Sisti; Dennis C. Liotta 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 243 KB

Al~tract: A pyrimidine moiety was tethered at the 3'-~-position of D-threo-furanosides. By carefully controlling the reaction conditions, pyrimidine bases can be delivered to the anomeric center to give of ~-pyrimidine nucleosides in good yield and with complete stereocontrol.