Abstract
Facile annulation of benzazepines onto furano-sugars has been achieved through Pd-catalyzed intramolecular cyclization. Using diisopropylidene d -glucose as a starting material, the first chiron approach to furobenzazepines in both cis and trans forms selectively introduced a 7-membered azepine ring linearly fused to a sugar nucleus. Cleavage of the sugar ring of the tricyclic derivatives provide a convenient route for entry into chiral functionalized 2-benzazepines, viz. 15 from 12a , and 16 from 14 .
Key words
furans - azepines - cyclizations - palladium - carbohydrates
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