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Palladium-catalyzed asymmetric alkoxycarbonylation of allyl phosphates

โœ 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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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


Palladium-catalyzed alkoxycarbonylation
โœ Soufiane El Houssame; Larbi El Firdoussi; Smail Allaoud; Abdellah Karim; Yves Ca ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 158 KB

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 โค, โฅ-unsaturated esters a