Simple synthesis of 4-hydroxycyclohexanone
โ Scribed by Radlick, Phillip.; Crawford, Herschel T.
- Book ID
- 120523726
- Publisher
- American Chemical Society
- Year
- 1972
- Tongue
- English
- Weight
- 163 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
We have developed a stereoselective route to 13-hydroxycyclohexanones using the aldol reaction, the Takai alkylidenation, a novel anionic oxy-Cope rearrangement of acyclic enol ethers and an intramolecular aldol reaction. The stereoselectivity of the acid-induced, 6-(enolendo)-exo-trig, intramolecul
Stereoselective Synthesis of ฮฒ-Hydroxycyclohexanones. -A stereoselective route to ฮฒ-hydroxycyclohexanones is reported. Thus Takai alkylidenation of the aldol (I) followed by desilylation and a novel anionic oxy-Cope rearrangement provides an enolate which undergoes 6-(enolendo)-exo-trig cyclization