Tetrahedron Letters p. 1163 - 1166 (1985)
Update date:2022-08-05
Topics:
Burke
Armistead
Fevig
An enantioselective synthesis of the tetrahydropyran 'left-wing' of the ionophore X-14547A is described, wherein stereoselective 1,2-carbonyl additions and an oxapyranone-to-dihydropyran enolate Claisen rearrangement are key stereocontrol elements.
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Doi:10.1016/S0040-4039(00)89176-5
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(2012)Doi:10.1016/j.poly.2005.10.022
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(1985)Doi:10.1246/cl.1989.459
(1989)
