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Volumn , Issue 36, 2011, Pages 7324-7330

The shortest strategy for generating phosphonate prodrugs by olefin cross-metathesis - Application to acyclonucleoside phosphonates

Author keywords

Acyclonucleoside phosphonates; Antiviral agents; Drug design; Medicinal chemistry; Metathesis; Phosphonate synthons; Prodrugs

Indexed keywords


EID: 82955223239     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201101111     Document Type: Article
Times cited : (19)

References (77)
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    • HDP-OH was synthesized following the Hostetler protocol by mesylation of palmityl alcohol, and substitution of the subsequent mesylate with deprotonated 1,3-propandiol.
    • HDP-OH was synthesized following the Hostetler protocol by mesylation of palmityl alcohol, and substitution of the subsequent mesylate with deprotonated 1,3-propandiol., G. D. Kini, J. R. Beadle, H. Xie, K. A. Aldern, D. D. Richman, K. Y. Hostetler, Antiviral Res. 1997, 36, 43-53.
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    • Kini, G.D.1    Beadle, J.R.2    Xie, H.3    Aldern, K.A.4    Richman, D.D.5    Hostetler, K.Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.