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Synthesis of spacered cyclopropyl nucleoside analogues as potential antiviral agents

✍ Scribed by René Csuk; Anja Kern


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
969 KB
Volume
55
Category
Article
ISSN
0040-4020

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✦ Synopsis


Novel spaeered cyclopropane nucleoside analogues possessing both a hydroxyethyl group and an additional methylene spacer between the base and the ring were synthesized starting from 3-buten-l-ol. After tetrahydropyranylation, eyelopropanation, and reduction the target molecules were obtained by Mitsunobu reactions followed by two consecutive deprotection steps.


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