4.6 Article

Cobalt-Catalyzed E-Selective Isomerization of Alkenes with a Phosphine-Amido-Oxazoline Ligand

Journal

ACS OMEGA
Volume 5, Issue 20, Pages 11655-11670

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.0c00951

Keywords

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Funding

  1. NSFC [21801191, 21572163, 21873074]
  2. Wenzhou Science & Technology Bureau [G20180016]
  3. College Students Innovation and Entrepreneurship Training Program [JWSC2018079]
  4. Laboratory open project of Wenzhou University [JW19SK65]

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An efficient method to access (E)-trisubstituted alkenes is reported via cobalt-catalyzed isomerization of 1,1-disubstituted alkenes using a phosphine-amido-oxazoline ligand. The reaction could also convert mono- and 1,2-disubstituted alkenes to (E)-internal alkenes with benzylic selectivity. This protocol is atom-economy and operationally simple and uses readily available starting materials with good functional tolerance. This catalytic system could be scaled up to gram scale smoothly with a catalyst loading of 0.1 mol %.

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