Sodium Borohydride??Nickel Chloride??Methanol Catalytic System for Regioselective Reduction of Electron??Rich Conjugated Dienes and Reductive Cleavage of Allyl …
…, ZR Zhang, L Huang, LW Xu, HF Jiang
Index: Yin, Biao-Lin; Cai, Cong-Bi; Lai, Jin-Qiang; Zhang, Ze-Ren; Huang, Li; Xu, Li-Wen; Jiang, Huan-Feng Advanced Synthesis and Catalysis, 2011 , vol. 353, # 18 p. 3319 - 3324
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Citation Number: 2
Abstract
Abstract The regioslective reduction of electron-rich dienes to monoolefins and the reductive cleavage of allyl esters were fulfilled by employing a sodium borohydride-nickel chloride- methanol catalytic system with exceedingly simple manipulations and high functional group tolerability. Both of the reductive reactions may involve π-allylnickel intermediates generated from fresh nickel boride.
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