The Synthesis of β,γ- and α,β-Unsaturated Aldehydes via Polyene Epoxides
✍ Scribed by Michael Rosenberger; William Jackson; Gabriel Saucy
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- German
- Weight
- 618 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A substitute for the Darzens glycidic ester synthesis for converting unsaturated ketones or aldehydes into the homologated β,γ‐ or α,β‐unsaturated aldehydes employing sulfur ylides is described. The carbonyl group is converted into the unsaturated oxirane which is then rearranged to the new aldehyde. High yields of isomerically pure aldehydes are available by this method and the process is of practical importance in the conversion of β‐ionone into the β‐C~14~‐aldehyde, a key intermediate in the Isler synthesis of vitamin A. The efficient preparation of α‐ and β‐cyclocitral by the novel process is also described.
📜 SIMILAR VOLUMES
## Abstract The direct organocatalytic enantioselective epoxidation of α,β‐unsaturated aldehydes with different peroxides is presented. Proline, chiral pyrrolidine derivatives, and amino acid‐derived imidazolidinones catalyze the asymmetric epoxidation of α,β‐unsaturated aldehydes. In particular, p
The oxidation of aldehydes to a@-unsaturated aldehydes has been performed by a sequence of reactions involving conversion into aldimines, chlorination at the a-position to form a-chloroaldimines, base-induced dehydrochlorination and h drol sis The four-step transformation can be executed without iso