1986
DOI: 10.1002/chin.198652095
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J. E. BALDWIN,
R. M. ADLINGTON,
J. C. BOTTARO
et al.

Abstract: Abstract The conversion (IIId) ‐ (VIII) exemplifies the use of the title compounds (III) [prepared from (I)] as acyl‐anion equivalents: anions of type (IV) generated from aldehydes (IIId)‐(IIIg) are treated with an electrophile such as (V) to yield (VI); subsequent tautomerization [‐ (VII)] and hydrolysis provides the target compound (VIII).

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