An expeditious route to carbocyclic nucleosides:(−)-aristeromycin and (−)-carbodine

F Burlina, A Favre, JL Fourrey, M Thomas

文献索引：Burlina, Fabienne; Favre, Alain; Fourrey, Jean-Louis; Thomas, Martial Bioorganic and Medicinal Chemistry Letters, 1997 , vol. 7, # 3 p. 247 - 250

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被引用次数: 39

摘要

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... The readily available bicyclic lactone (−)-1 was transformed into diacetate (−)-2 which served in an expeditious route to (−)-aristeromycin (3a) and (−)-carbodine (3b) in acceptable yields. ... In both series 11 is less polar than 12 (CH 2 Cl 2 /Methanol system).