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Functionalized 2-azabicyclo[3.3.1]nonanes. III.1 reductive rearrangement of an hexahydro-2-oxopyrano[3,2-b]pyridine

✍ Scribed by Joan Bosch; Josep Bonjoch; Isabel Serret


Book ID
104220586
Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
143 KB
Volume
23
Category
Article
ISSN
0040-4039

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Functionalized 2-azabicyclo[3.3.1]nonane
✍ Josep Bonjoch; Josefina Quirante; Isabel Serret; Joan Bosch πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 153 KB

The reaction of the pyrrolidine enamine derived from l-benzyl-2,5\_piperidinedione with acrolein afforded a 3,6,9-trifunctionalized 2-azabicyclo[3.3.1] nonane system, which could be isolated as a stable ketone hydrate.