期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 65, 期 24, 页码 8340-8347出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo001207d
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Racemic (+/-)-3,3'-bis(diphenylphosphinyl)-1,1'-dimethyl-2,2'-biindole (Ic) (N-Me-2-BINPO) and (+/-)-3,3'-bis(diphenylphosphinyl)-1, 1'-bis(methoxymethyl)-2,2'-biindole (Id) (N-MOM-2-BINPO) were synthesized in satisfactory yields following a three-step reaction sequence,starting from indole. Resolution of racemic Ic and Id was achieved through fractional crystallization of their diastereomeric adducts with optically active dibenzoyl tartaric acids, followed by alkaline decomplexation of the diastereomerically pure salts. Their trichlorosilane reduction gave enantiopure phosphines (+)- and (-)-(la) (N-Me-2-BINP) and (+)- and (-)-(lb) (N-MOM-2-BINP). The electrochemical oxidative potential of la and Ib was found to be 0.52 and 0.60 V, respectively. Both the enantiomers of(la) were tested as ligands of Ru(II) in asymmetric hydrogenation reactions of alpha- and beta -oxoesters. Reactions were found to be outstandingly fast and enantioselection quite good. Comparative kinetic experiments on the hydrogenation reaction of methyl acetoacetate carried out with la, Ic, BINAP, and other biheteroaromatic diphosphines as ligands of Ru(II) demonstrated that all the reactions follow a first-order kinetic. A Linear relationship was found between the kinetic constant log and the electrochemical oxidative potential of the diphosphine ligand.
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