208179-45-7Relevant articles and documents
A highly efficient synthesis of the antiviral agent (+)-cyclaradine involving the regioselective cleavage of epoxide by neighboring participation
Katagiri, Nobuya,Matsuhashi, Yumiko,Kokufuda, Hideaki,Takebayashi, Masahiro,Kaneko, Chikara
, p. 1961 - 1964 (2007/10/03)
(+)-Cyclaradine, carbocyclic arabinofuranosyladenine having anti-HSV activity, has been synthesized from (-)-2-azabicyclo[2.2.1]hept-5-en-3-one in only seven steps. The method involves the novel ring cleavage of epoxide by neighboring participation.