An efficient route to 3-substituted cyclobutanone derivatives
โ Scribed by George W. Kabalka; Min-Liang Yao
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 126 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
An efficient route to 3-(hydroxymethyl)cyclobutanone acetals via a [2+2] cycloaddition reaction is reported. The dramatic effect of different diol acetals on benzyl deprotection is discussed. Efficient synthesis of two synthetically useful intermediates, 3-methylenecyclobutanone acetal and 3-(bromomethyl)cyclobutanone, are provided.
๐ SIMILAR VOLUMES
The novel 4-chloro-2,5-dimethoxybenzaldehyde 1 has been prepared and converted in only three steps to 5-acetoxy-7-carboethoxy-3-chloro-l,4-naphthaquinone 4. Subsequent Diels-Alder reaction affords a tetracyclic enol ether 2 in a regiospecific manner. Failure of simple juglones to undergo regiospecif
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