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Oxidative degradation of L-ascorbic acid acetals to 2′, 3′-dideoxy-3′-oxaribofuranosides. Synthesis of enantiomerically pure 2′, 3′-dideoxy-3′-oxacytidine …

BR Belleau, CA Evans, HLA Tse, H Jin, DM Dixit…

Index: Tetrahedron Letters, , vol. 33, # 46 p. 6949 - 6952

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Citation Number: 39

Abstract

... JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. Tetrahedron Letters. Volume 33, Issue 46, 10 November 1992, Pages 6949–6952. The International Journal for the Rapid Publication of Preliminary. ...

L-. beta.-(2S, 4S)-and L-. alpha.-(2S, 4R)-dioxolanyl nucleosides as potential anti-HIV agents: asymmetric synthesis and structure-activity relationships

[Kim; Schinazi; Shanmuganathan; Jeong; Beach; Nampalli; Cannon; Chu Journal of Medicinal Chemistry, 1993 , vol. 36, # 5 p. 519 - 528]

Potent anti-HIV and anti-HBV activities of (−)-L-β-dioxolane-C and (+)-L-β-dioxolane-T and their asymmetric syntheses.

[Tetrahedron Letters, , vol. 33, # 46 p. 6899 - 6902]

Oxidative degradation of L-ascorbic acid acetals to 2′, 3′-dideoxy-3′-oxaribofuranosides. Synthesis of enantiomerically pure 2′, 3′-dideoxy-3′-oxacytidine …

Abstract

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