๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A synthesis of ynolates via the cleavage of ester dianions

โœ Scribed by Mitsuru Shindo


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
199 KB
Volume
38
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


Novel synthesis of ynolates via the clea
โœ Mitsuru Shindo; Yusuke Sato; Kozo Shishido ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 690 KB

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

ChemInform Abstract: Novel Synthesis of
โœ M. SHINDO; Y. SATO; K. SHISHIDO ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 35 KB ๐Ÿ‘ 1 views

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

Lactone synthesis via the intramolecular
โœ Russell J. Sims; Samuel A. Tischler; Larry Weiler ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 192 KB

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

Synthesis of o-halogenophenylacetylenes
โœ H. Hommes; H.D. Verkruijsse; L. Brandsma ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 121 KB

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.