Palladium-catalyzed asymmetric alkoxycarbonylation of allyl phosphates
โ Scribed by Yasushi Imada; Masaru Fujii; Yasushi Kubota; Shun-Ichi Murahashi
- Book ID
- 104258274
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 222 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Palladium-catalyzed alkoxycarbonylation of allyl phosphates proceeds with high efficiency affording the corresponding [3,y-unsaturatod esters stereoselectively with inversion of configuration at the allylic carbon center. Palladium complexes bearing chiral monodentate phosphine ligands are effective catalysts for asymmetric allylic carbonylation of cyclohex-2-en-l-yl phosphates 1 to give optically active cyclohex-2-ene-1--carboxylates 2 in moderate enantiomeric excesses.
๐ SIMILAR VOLUMES
The palladium-catalyzed alkoxycarbonylation of allyl carbonates and allyl chlorides derivatives from terpenic olefins was carried out under atmospheric pressure of carbon monoxide and at moderate temperature. The reaction offers a very good method for the preparation of new โค, โฅ-unsaturated esters a