Beckmann reductive, ring expansion

Ozonolysis of alkene 446 in the presence of acetaldehyde afforded diketone 448 through the intermediacy of 447. Ring expansion through Beckmann rearrangement took place when bis-oxime 449 was mesylated and warmed in aqueous tetrahydrofuran (THF). The bis-lactam so formed gave piperidinediol 450 on reduction with lithium aluminium hydride, and this compound was transformed into ( )-sparteine by treatment with triphenylphosphine, CCI4, and triethylamine (Scheme 105) <20050BC1557>. 

During the synthesis of ligands for the vesicular acetylcholine transporter, a octahy-droquinoline nucleus 361 was prepared via a ring-expansion rearrangement followed by a hydride reduction (equation 140). The yield was moderate but only one lactam 360 was produced by the Beckmann rearrangement. 

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