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

✍ Scribed by Fabienne Burlina; Alain Favre; Jean-Louis Fourrey; Martial Thomas

Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
251 KB
Volume
7
Category
Article
ISSN
0960-894X

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✦ Synopsis

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.

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