𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Stereoselective Synthesis of 6-Methyl-9-(2-deoxy-β-D-erythro- pentofuranosyl)purine.

✍ Scribed by J. E. ANDERSON-MCKAY; G. W. BOTH; G. W. SIMPSON

Book ID
112040536
Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
27
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Cytostatic 6-Arylpu
ChemInform Abstract: Cytostatic 6-Arylpurine Nucleosides. Part 2. Synthesis of Sugar-Modified Derivatives: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-, 9-(5-Deoxy-β-D-ribofuranosyl)- and 9-(2,3-Dihydroxypropyl)-6-phenylpurines.
✍ Michal Hocek; Antonin Holy; Ivan Votruba; Hana Dvorakova 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 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

ChemInform Abstract: Synthesis of 9-(2-D
ChemInform Abstract: Synthesis of 9-(2-Deoxy-β-D-ribofuranosyl)purine-2-thione.
✍ Harry P. Rappaport 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 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

Acidic hydrolysis of 6-substituted 9-(2-
Acidic hydrolysis of 6-substituted 9-(2-deoxy-β-d-erythro- pentofuranosyl) purines and their 9-(1-alkoxyethyl) counter-parts: kinetics and mechanism.1
✍ Mikko OivanXXXn; Harri Lönnberg; Xiao-xiong Zhou; Jyoti Chattopadhyaya 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 543 KB

The rate constants for the hydrolysis of several rubrt mted 9-(2-deoxy-B-D-erythro-pentofurenosyl)purines end 9-(l-rlkoxyethvl)purines firm ii measured at different concentrrtionb of-oxoniua ion. The effects that varying the polar nature of the l lkoxy group exerts on the hydrolysis of unsubstituted