It is possible to isolate nitrogen-containing compounds using the B�chner Curtius Schlotterbeck reaction.
2.
The B�chner Curtius Schlotterbeck reaction used to insert a methylene bridge between a halogen and a cabonyl carbon of an acyl halide
3.
Steric effects of the alkyl substituents on the carbonyl reactant have been shown to affect both the rates and yields of B�chner Curtius Schlotterbeck reaction.
4.
The B�chner Curtius Schlotterbeck reaction can also be used to insert a methylene bridge between a carbonyl carbon and a halogen of an acyl halide.
5.
The B�chner Curtius Schlotterbeck reaction can be used to facilitate one carbon The B�chner ring expansion reactions utilizing diazoalkanes have proven to be synthetically useful as they can not only be used to form 5-and 6-membered rings, but also more unstable 7-and 8-membered rings.
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