Concurrent ring opening and halogenation of spiroketals

DOI: 10.1016/S0040-4039(99)00827-8

Source and publish data:

Tetrahedron Letters p. 4655 - 4658 (1999)

Update date:2022-08-04

Topics:

Authors:

LaCour, Thomas G.

Fuchs Fuchs

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Article abstract of DOI:10.1016/S0040-4039(99)00827-8

Ring opening of various spiroketals with triphenylphosphine dihalides under neutral conditions produced ω-halo-enolethers in good to excellent yield. The method transformed even the very stable spiroketal of hecogenin acetate at temperatures below any previously reported for such isomerative opening.

Full text of DOI:10.1016/S0040-4039(99)00827-8

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