54966-44-8Relevant articles and documents
Ligand-Controlled Palladium-Catalyzed Alkoxycarbonylation of Allenes: Regioselective Synthesis of α,β- and β,γ-Unsaturated Esters
Liu, Jie,Liu, Qiang,Franke, Robert,Jackstell, Ralf,Beller, Matthias
supporting information, p. 8556 - 8563 (2015/07/15)
The palladium-catalyzed regioselective alkoxycarbonylation of allenes with aliphatic alcohols allows to produce synthetically useful α,β- and β,γ-unsaturated esters in good yields. Efficient selectivity control is achieved in the presence of appropriate ligands. Using Xantphos as the ligand, β,γ-unsaturated esters are produced selectively in good yields. In contrast, the corresponding α,β-unsaturated esters are obtained with high regioselectivity in the presence of PPh2Py as the ligand. Preliminary mechanistic studies revealed that these two catalytic processes proceed by different reaction pathways. In addition, this novel protocol was successfully applied to convert an industrially available bulk chemical, 1,2-butadiene, into dimethyl adipate, which is a valuable feedstock for polymer and plasticizer syntheses, with high yield and TON (turnover number).
Domino catalysis: Palladium-catalyzed carbonylation of allylic alcohols to β,γ-unsaturated esters
Liu, Qiang,Wu, Lipeng,Jiao, Haijun,Fang, Xianjie,Jackstell, Ralf,Beller, Matthias
supporting information, p. 8064 - 8068 (2013/08/23)
Make it green: The Pd-catalyzed carbonylation of allylic alcohols with aliphatic alcohols represents a cost-effective, salt-free, and atom-economic carbonylation process generating water as the sole by-product. Mechanistic studies uncovered a new domino C-O coupling/carbonylation reaction pathway. Copyright
Palladium-Catalyzed Carbonylation of Allyl Alcohols in the Presence of Phenols
Satoh, Tetsuya,Ikeda, Masahiro,Kushino, Yuichi,Miura, Masahiro,Nomura, Masakatsu
, p. 2662 - 2664 (2007/10/03)
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