-2-oxopropyl]triphenylarsonium bromide 8 with 7-methoxy-3,7-dimethyloctanal 10 in the presence of a base gave bis(1-methylethyl) 4,7-dihydroxy-2-(6-methoxy-2,6-dimethylheptyl)-3,5,7-cycloheptatriene-1,3-dicarboxylate 7b. The formation of 7b can be explained by a number of consecutive steps. The mech
ChemInform Abstract: An Unusual Condensation of Alkyl 3-Oxo-4-(triphenylarsoranylidene) butanoate with Aldehydes; Synthesis of Symmetrical Substituted 1,3,5- Cycloheptatrienes.
β Scribed by C. M. MOORHOFF
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
An Unusual Condensation of Alkyl 3-Oxo-4-(triphenylarsoranylidene) butanoate with Aldehydes; Synthesis of Symmetrical Substituted 1,3,5-Cycloheptatrienes.
-Aldehydes and 2 equiv. of arsonium ylides (I) undergo a unique reaction to yield the title compounds (III), potentially useful intermediates in organic synthesis.
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