The reaction of benzene-1,2-diol with various propargylic carbonates in the presence of a palladium catalyst and various chiral ligands afforded the corresponding 2-alkylidene-3-alkyl-2,3-dihydrobenzodioxins in quite good yields and enantioselectivities of up to 97%. The highest enantiomeric ex- [a]
✦ LIBER ✦
Asymmetric Palladium-Catalyzed Annulation of Benzene-1,2-diol and Racemic Secondary Propargylic Carbonates Bearing Two Different Substituents.
✍ Scribed by Norbert Dominczak; Celine Damez; Bouchra Rhers; Jean-Robert Labrosse; Paul Lhoste; Boguslaw Kryczka; Denis Sinou
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 32 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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