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Synthesis 2008(20): 3209-3218
DOI: 10.1055/s-0028-1083140
DOI: 10.1055/s-0028-1083140
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
A New Route for the Preparation of Succinates
Further Information
Received
20 May 2008
Publication Date:
25 September 2008 (online)
Publication History
Publication Date:
25 September 2008 (online)

Abstract
Succinates of the tertiary hydroxy group having a formyl group in the structure were conveniently synthesized by oxidative cleavage of dihydropyrans prepared from lactones via coupling of ketene acetal triflates and zinc homoenolates.
Key words
succinates - dihydropyrans - esters - lactones - dihydroxylations
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