Synlett 2012; 23(10): 1489-1492
DOI: 10.1055/s-0031-1290670
letter
© Georg Thieme Verlag Stuttgart · New York

A Modular, Stereoselective Approach to Spiroketal Synthesis

Michael T. Crimmins*
,
Adam M. Azman
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Publikationsverlauf

Received: 10. Februar 2012

Accepted after revision: 30. März 2012

Publikationsdatum:
29. Mai 2012 (online)


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Abstract

A highly convergent and flexible synthetic approach to stereochemically defined spiroketals is reported. Substituents can be incorporated at various positions around the spiroketal framework without significant disruption to the synthetic scheme. The approach has been exploited to prepare the spiroketal fragment of milbemycin β14.

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