An expeditious route to carbocyclic nucl
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Fabienne Burlina; Alain Favre; Jean-Louis Fourrey; Martial Thomas
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Article
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1997
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Elsevier Science
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English
⚖ 251 KB
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.