Beilstein Journal of Organic Chemistry (Dec 2012)

Stereoselective synthesis of tetrasubstituted alkenes via a sequential carbocupration and a new sulfur–lithium exchange

  • Andreas Unsinn,
  • Cora Dunst,
  • Paul Knochel

DOI
https://doi.org/10.3762/bjoc.8.248
Journal volume & issue
Vol. 8, no. 1
pp. 2202 – 2206

Abstract

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We have designed a new sequential carbocupration and sulfur–lithium exchange that leads stereo- and regioselectively to trisubstituted alkenyllithiums. Subsequent trapping with various electrophiles yields tetrasubstituted olefins with good control of the double-bond geometry (E/Z ratio up to 99:1). The novel sulfur–lithium exchange could be extended to the stereoselective preparation of Z-styryl lithium derivatives with almost complete retention of the double-bond geometry.

Keywords