1989
DOI: 10.1002/chin.198925286
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ChemInform Abstract: Synthesis of 3′‐Cyano‐3′‐deoxy‐β‐D‐arabino‐nucleosides.

Abstract: The compounds (III) mentioned in the title are prepared by regioselective ring cleavage of the lyxo‐epoxides (I) with cyanodiethylaluminum (II).

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“…17 The same author used hydrazoic acid as 1,3-dipole and a carbodiimide as dipolarophile, generated from AZT, for the elaboration of compound 6, which also exhibited moderate activity against HIV-1. 18 The series of products 7 were prepared and tested as antiviral HIV agents, the most active being R 1 = Bu t (Me) 2 Si-, R 2 , R 4 = H, R 3 = CONMe 2 . 19 Phosphasugar Fig.…”
Section: Azidesmentioning
confidence: 99%
See 1 more Smart Citation
“…17 The same author used hydrazoic acid as 1,3-dipole and a carbodiimide as dipolarophile, generated from AZT, for the elaboration of compound 6, which also exhibited moderate activity against HIV-1. 18 The series of products 7 were prepared and tested as antiviral HIV agents, the most active being R 1 = Bu t (Me) 2 Si-, R 2 , R 4 = H, R 3 = CONMe 2 . 19 Phosphasugar Fig.…”
Section: Azidesmentioning
confidence: 99%
“…17 The same author used hydrazoic acid as 1,3-dipole and a carbodiimide as dipolarophile, generated from AZT, for the elaboration of compound 6, which also exhibited 75 moderate activity against HIV-1. 18 The series of products 7…”
mentioning
confidence: 99%