A new indirect application of aggregative activation: Synthesis of esters by cobalt-catalyzed carbonylation of aryl, heterocyclic, and vinyl halides under atmospheric pressure
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Marchal, J
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UNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCEUNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCE
Marchal, J
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Bodiguel, J
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UNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCEUNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCE
Bodiguel, J
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Fort, Y
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Caubere, P
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UNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCEUNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCE
Caubere, P
[1
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[1] UNIV NANCY 1,FAC SCI,INCM FU CNRS 0008,URA CNRS 457,LAB CHIM ORGAN 1,F-54506 VANDOEUVRE NANCY,FRANCE
Sun lamp illuminated alkoxycarbonylation of aryl, heteroaryl, and vinyl halides was performed under atmospheric pressure of CO in the presence of a cobalt catalyst in situ generated from Co(OAc)(2). Illumination through a Pyrex flask was sufficient to catalyze the reaction. This process avoids the use of Co-2(CO)(8) and excess CH3I, which were required in the earlier procedure. A S-RN(1) mechanism is proposed.