3, [3'-Dihydroxy carboxylic acids and esters, readily prepared from dibromofluoroacetate and aldehydes, underwent deoxygenation, followed by elimination of aldehyde by the action of vanadium(V) trichloride oxide at the reflux temperature of chlorobenzene for 1 h to afford the Z isomers of oc-fluoro-
Reaction of carbon dioxide with trialkylalkynyl borates — a novel method for the synthesis of stereospecific α,β-unsaturated acids
✍ Scribed by Deng Min-zhi; Tang Yong-ti; Xu Wei-hua
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 136 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Carboxylation of lithium trialkylalkynylborate can take place under favourable conditions.
Protonation of the reaction product yields (Z)-a,P-unsaturated acid.
Quite a variety of electrophiles have been used in reaction with alkynylborates. Among these are carboxylic acids, iodinel, simple alkylating agents, such as alkyl halides or tosylates2, metal stablized cations 3 , acid pyridinium saits 4 5 6
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