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Palladium-catalyzed regioselective reactions of α-acetoxy-β,γ-unsaturated nitriles and γ-acetoxy-α,β-unsaturated ester with nucleophiles
✍ Scribed by Jiro Tsuji; Hiroaki Ueno; Yuichi Kobayashi; Hiroshi Okumoto
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 120 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
e-Acetoxy-8,y-unsaturated nitriles react at room temperature with malonates and acetoacetates in the presence of palladium-phosphine complexes as a catalyst to give y-substituted a,8-unsaturated nitriles selectively. Also yacetoxy-a,8-unsaturated ester was attacked at y-position by malonate.
📜 SIMILAR VOLUMES
## Abstract Treatment of 3‐methylamino‐5‐phenylthiophene with α,β‐unsaturated esters, __i.e.__, methyl acrylate, (__E__)‐methyl crotonate, diethyl fumarate, diethyl maleate and ethyl propiolate, in tetrahydrofuran for several days at reflux gave 1‐methyl‐3,4‐dihydrothieno[2,3‐__e__]pyridin‐2‐ones *