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首页> 外文期刊>Organometallics >Olefin metatheses in metal coordination spheres: a new approach to steric shielding in dirhenium sp carbon chain complexes of the formula (eta(5)-C5Me5)-Re(NO)(PR3)(C CC CC CC C)(R3P)(ON)Re(eta(5)-C5Me5)
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Olefin metatheses in metal coordination spheres: a new approach to steric shielding in dirhenium sp carbon chain complexes of the formula (eta(5)-C5Me5)-Re(NO)(PR3)(C CC CC CC C)(R3P)(ON)Re(eta(5)-C5Me5)

机译:金属配位领域中的烯烃复分解:分子式为(eta(5)-C5Me5)-Re(NO)(PR3)(C CC CC CC C)(R3P)(ON)的Sp碳链络合物的空间屏蔽新方法)Re(eta(5)-C5Me5)

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Reaction of chiral racemic [(eta(5)-C5Me6)Re(NO)(NCCH3)(CO)]+BF4- and the olefin-containing phosphine Ph2P(CH2)(6)CH = CH2 (2-butanone, reflux) gives [(eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(CO)]+BF4- (95%), which is reduced (LiAlH4) to the phosphine methyl complex (eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(CH3) (92%).,Reactions with HBF4.OEt2/chloroben-zene, HCequivalent toCCequivalent toCSiMe(3), and t-BuOK give (eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(C equivalent to CC equivalent to CSiMe3) (two steps, 96%/81%). Desilylation (wet n-Bu4N+F-) yields a butadiynyl complex (88%), which is coupled (Cu(OAc)(2)/pyridine) to the mu-octatetraynediyl complex (eta(5)-C5Me5)-Re(NO)(PPh2(CH2)(6)CH=CH2)(C equivalent to CC equivalent to CC equivalent to CC equivalent to C)(H2C=CH(CH2)(6)PPh2)(ON)Re(eta(5)-C5Me5) (16, 63%), believed to be a mixture of diastereomers. The reaction of 16 and Grubbs' catalyst, Ru(=CHPh)(PCY3)(2)(Cl)(2), gives (eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH=CH)(Cequivalent to CC equivalent to CC equivalent to C)- ((CH2)(6)PPh2)(ON)Re(eta(5)-C5Me5) (17, 77-84%) as a mixture of isomers. However, the hydrogenation of 17 to the target molecule (eta(5)-C5Me5)Re(NO)(PPh2(CH2)(7))(Cequivalent toCCequivalent toCCequivalent toCCequivalent toC)((CH2)(7)PPh2)(ON)Re(eta(5) -C5Me5) (18), while sometimes successful, could not be scaled or effected in a reproducible manner. [References: 50]
机译:手性外消旋[(eta(5)-C5Me6)Re(NO)(NCCH3)(CO)] + BF4-与含烯烃的膦Ph2P(CH2)(6)CH = CH2(2-丁酮,回流)的反应得到[(eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(CO)] + BF4-(95%),将其还原(LiAlH4)为膦甲基络合物( eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(CH3)(92%)。,与HBF4.OEt2 /氯代苯的反应,HC等效于CSiMe(3), t-BuOK给出(eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH2)(C等效于CC等效于CSiMe3)(两步,96%/ 81%)。脱甲硅烷基化(湿n-Bu4N + F-)生成丁二炔基复合物(88%),该复合物(Cu(OAc)(2)/吡啶)与mu-octatetraynediyl复合物(eta(5)-C5Me5)-Re( NO)(PPh2(CH2)(6)CH = CH2)(C等同于CC等同于CC等同于CC等同于C等同于CC)(H2C = CH(CH2)(6)PPh2)(ON)Re(eta(5) -C5Me5)(16,63%),被认为是非对映异构体的混合物。 16与Grubbs的催化剂Ru(= CHPh)(PCY3)(2)(Cl)(2)的反应得到(eta(5)-C5Me5)Re(NO)(PPh2(CH2)(6)CH = CH)(相当于CC等于相当于C的CC)-((CH2)(6)PPh2)(ON)Re(eta(5)-C5Me5)(17,77-84%)作为异构体的混合物。但是,将17氢化为目标分子(eta(5)-C5Me5)Re(NO)(PPh2(CH2)(7))(相当于C相当于C相当于C相当于C相当于C)(((CH2)(7)PPh2)(ON) Re(eta(5)-C5Me5)(18)有时会成功,但无法缩放或以可再现的方式实现。 [参考:50]

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