A synthesis of ynolates via the cleavage of ester dianions
โ Scribed by Mitsuru Shindo
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 199 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A new method for ynolate synthesis via the cleavage of ester dianions has been developed. The key intermediates, ester dianions, generated from ct-bromocarboxylic acid ester enolates via lithiumhalogen exchange turned out to be so labile that they were cleaved rapidly to give ynolates.
๐ SIMILAR VOLUMES
Ynolates have been synthesized via the thermally-inducedcleavage of ester dianions. The key intermediates, ester dianions, were generated from ~t -bromocarboxylic acid ester enolates via lithium halogen exchange, ot,~-Dibromocarboxylic acid ester also gives lithium amide free ynolates by addition of
Novel Synthesis of Ynolates via the Cleavage of Ester Dianions: ฮฑ-Bromo and ฮฑ,ฮฑ-Dibromo Esters as Precursors. -Thermal cleavage of ester dianions generated from readily available ฮฑ-bromo-and ฮฑ,ฮฑ-dibromo esters offers a new and convenient method to prepare lithium ynolates. The ynolates react with al
Long chain m-halo B-keto esters yield macrocyclic B-keto lactones. British Columbia, Vancouver, B.C., Canada V6T lY6 undergo intramolecular alkylation via the dianions to Since the isolation of exaltolide (pentadecanolide) by Kerschbauml fifty-five years ago, a large number of macrocyclic lactones h
The o-halogenophenylacetylenes o-iodophenylacetylene, o-bromophenylacetylene and o-chlorophenylacetylene can be prepared by regiospecific reaction of iodine, bromine, and hexachloroethane respectively with the dianion of phenylacetylene.