Tandem [2, 3]-sigmatropic rearrangement of sulfonium ylides and bromine allylic rearrangement on a 4-methoxy-2-pyrone derivative

P De March, M Moreno-Manas…

Index: March, Pedro de; Moreno-Manas, Marcial; Roca, J. L. Journal of Organic Chemistry, 1988 , vol. 53, # 21 p. 5149 - 5151

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Citation Number: 6

Abstract

The general rearrangement is depicted in Scheme I (1-2). If tautomer 3 is more stable than tautomer 2, conversion of 2 into 3 can occur either directly under the [2, 3]-sigmatropic rearrangement experimental conditions or in a subsequent step as we have already shown? However, at the best of our knowledge no X groups different from hydrogen have been used in the transformations 1-3. Such an overall process would imply a novel and important ...