Enol Tosylates as Viable Partners in
Pd-Catalyzed Cross-Coupling Reactions

Steinhuebel, Dietrich; Baxter, Jenny M.; Palucki, Michael; Davies, Ian W.

doi:10.1021/jo051590s.s001

jo051590s_si_001.pdf (103.17 kB)

Enol Tosylates as Viable Partners in Pd-Catalyzed Cross-Coupling Reactions

journal contribution

posted on 2005-11-25, 00:00 authored by Dietrich Steinhuebel, Jenny M. Baxter, Michael Palucki, Ian W. Davies

Herein we demonstrate functionalized enol tosylates to be robust substrates that undergo Suzuki−Miyaura, Sonogashira, and Stille cross-coupling reactions to provide stereodefined trisubstituted unsaturated esters.

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esters Sonogashira stereodefined trisubstituted Stille Viable Partners Suzuki functionalized enol tosylates Enol Tosylates substrate Herein

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