Hemi-thioacetal pummerer reaction for the synthesis of gliovirin benzylic sulfide models

DOI: 10.1016/S0040-4039(98)02064-4

Source and publish data:

Tetrahedron Letters p. 9131 - 9134 (1998)

Update date:2022-07-31

Topics:

Authors:

Magnus, Philip

Mitchell, Ian S.

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Article abstract of DOI:10.1016/S0040-4039(98)02064-4

The cyclic hemithioacetal sulfoxide 15 readily undergoes the Pummerer reaction in the presence of carbon nucleophiles to give substitute benzylic sulfides in excellent yields.

Full text of DOI:10.1016/S0040-4039(98)02064-4

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