Detailed Information
Cited 0 time in 
Cited 0 time in 
Cited 0 time in
Metadata Downloads
Stereoselective Synthesis of Anti-Hepatitis B Drug, Entecavir, through Regio- and Stereoselective Epoxide Cleavage
- Issue Date
- 9월-2017
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- carbocyclic nucleoside; entecavir; hepatitis B; Stereoselective synthesis; titanium
- Citation
- ASIAN JOURNAL OF ORGANIC CHEMISTRY, v.6, no.9, pp.1213 - 1218
- Indexed
- SCIE
SCOPUS
- Journal Title
- ASIAN JOURNAL OF ORGANIC CHEMISTRY
- Volume
- 6
- Number
- 9
- Start Page
- 1213
- End Page
- 1218
- ISSN
- 2193-5807
- Abstract
- A stereoselective synthesis of entecavir, an anti-hepatitis B (HBV) drug, was accomplished by a regioselective isopropylidene cleavage, stereoselective Sharpless epoxidation, and Ti-III-mediated regio- and stereoselective epoxide cleavage as key steps.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Biotechnology > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.