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Rearrangement during reduction of cis-and trans-2-phenylcinnamic acids with lithium aluminium hydride

✍ Scribed by B.R. Brown; P.E. Brown

Publisher
Elsevier Science
Year
1963
Tongue
French
Weight
76 KB
Volume
4
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

The reduction of 2-phenyl-cis- and trans
The reduction of 2-phenyl-cis- and trans-cinnamic acids with lithium aluminum hydride. The equilibration of 2-phenyl-cis- and trans-cinnamyl alcohols and 1,2-diphenyl-2-propenol.
✍ T. Axenrod; E. Bierig; L.H. Schwartz 📂 Article 📅 1965 🏛 Elsevier Science 🌐 French ⚖ 224 KB

cis\_ or tmns\_cinnamic acid (I and II, respectively) undergoes rearrangement to l, Z-diphenyl-2-propenol (III) during lithium aluminum hydride reduction. This claim was based on the following experimental results.