𝔖 Bobbio Scriptorium
✦   LIBER   ✦

An asymmetric synthesis of (−)-carbovir

✍ Scribed by Masatoshi Asami; Jun Takahashi; Seiichi Inoue


Book ID
103976993
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
293 KB
Volume
5
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of Novel Carbovir Analogue.
✍ Aihong Kim; Joon Hee Hong 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 32 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.

A Short Synthesis of (−)-Carbovir
✍ Stefan Hildbrand; Thomas Troxler; Rolf Scheffold 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 German ⚖ 330 KB
ChemInform Abstract: A Concise Enantiose
✍ S. TANIMORI; M. TSUBOTA; M. HE; M. NAKAYAMA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

A Concise Enantioselective Pathway to Carbocyclic Nucleoside: Asymmetric Synthesis of Carbocyclic Moiety of Carbovir. -An enantioselective synthesis of cyclopentenol (VIII), an advanced intermediate for the preparation of carbovir, involving the Rh(II)-catalyzed intramolecular cyclopropanation of a

Enantioselective synthesis of the carboc
✍ Emmanuel Roulland; Claude Monneret; Jean-Claude Florent 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 156 KB

Enantioselective construction of the protected carbocycle moiety of the anti-HIV drug carbovir was achieved in 11 steps from (S)-(-)-ethyl lactate. The two key steps are a Claisen [3+3] sigmatropic rearrangement of (3S,4E)-3-(4-methoxy-phenoxymethyl)-hex-4-enoic acid dimethylamide and next, a ruthen