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Synthesis of ketenimine via (N-alkylimino)acylpalladium complex intermediate

โœ 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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โœฆ 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


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Total synthesis of (ยฑ)-anatoxin-a via N-
โœ Karen H Melching; Henk Hiemstra; Wim J Klaver; W.Nico Speckamp ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 254 KB

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