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Updated: Jun 20, 2026

Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
Synthesis of 5'-fluoro-2'-beta-methylneplanocin analogues
Hiroki Kumamoto1, Marina Kobayashi, Hiromichi Tanaka
1School of Pharmaceutical Sciences, Showa University, Tokyo 142-8555, Japan. kumamoto@pharm.showa-u.ac.jp
Abstract:
Synthesis of 5'-fluoro-2'-beta-methylneplanocin analogues (5) was carried out. The cyclopentenone 16 was prepared from methyl mannopyranoside by using ring closing metathesis, stereoselective introduction of methyl group, and seleno cyclization as representative steps. Introduction of a fluorine atom was conducted by electrophilic fluorination. Antiviral activity of 5 will also be presented.
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