Synthesis of ketenimine via (N-alkylimino)acylpalladium complex intermediate
โ Scribed by Yoshihiko Ito; Toshikazu Hirao; Nobuhiro Ohta; Takeo Saegusa
- Book ID
- 104243930
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 209 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Recently we have reported' that diaminocarbene Pd(I1) complex (2 is converted into carbodiimide in high yields when it is treated with base, such as butyllithium and potassiumtertbutoxide, or with Ag20. The formation of carbodiimide was reasonably explained by a mechanism involving b-elimination of aminoiminomethylpalladium complex (A in which Pd-H species is removed (eq 1
๐ SIMILAR VOLUMES
Anatoxin-a has been synthesized in 8 steps, starting from succinimide, 4-bromo-l--butene and dimethyl (2-oxopropyl)phosphonate, by employing as the key step an intramolecular reaction of an N-acyliminium precursor with an cu,&unsaturated ketone moiety, induced by saturated HCl in MeOH at -5OOC. Ana