Recently we reported on the reactions of cyclic g-diketones and carbethoxycycloalkanones with compound I under basic catalysis. 2 In monoglyme, the products obtained were, invariably a mixture of tautomers arising from protonation of an initially formed 1,6-adduct. In DMSO the products were derivab
Reactions of methyl β-vinylacrylate with β-dicarbonyl compounds--a new route to functionalized bridged ring systems
✍ Scribed by S. Danishefsky; G. Koppel; R. Levine
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 216 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The l,&addition of nucleophiles to activated butadienes was first demonstrated by Kohler and Butler (1) in the reaction of sodiomalonic ester with methyl B-vinylacrylate(1).
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## Abstract Palladium‐catalyzed tandem reactions of β‐(2‐bromophenyl)‐α,β‐unsaturated carbonyl compounds with 2‐hydroxyphenylboronic acid for the synthesis of benzo[__c__]chromenes are presented. This mild reaction allows formation of onecarbon–carbon bond and one carbon–oxygen bond in one pot.