CONJUGATE-ADDITION REACTIONS OF HIGHLY-FUNCTIONALIZED ARYL LITHIUM REAGENTS TO γ-SILYLOXY-α,β-UNSATURATED SULFONES: CONSEQUENCES OF THE STRUCTURE OF THE SULFONE MOIETY.

DOI: 10.1016/S0040-4039(00)92786-2

Source and publish data:

Tetrahedron Letters p. 1811 - 1814 (1980)

Update date:2022-08-02

Topics:

Authors:

Barton, D. L.

Conrad, P. C.

Fuchs, P. L.

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Article abstract of DOI:10.1016/S0040-4039(00)92786-2

The effect of sulfone structure (phenyl vs t-butyl) is compared in the conjugate-addition reactions of ortho substituted and ortho, ortho disubstituted aryl lithium reagents with γ-silyloxy-α,β-unsaturated sulfones.

Full text of DOI:10.1016/S0040-4039(00)92786-2

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