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马特森不对称同系化反应的催化版本研究。

Studies on a catalytic version of the Matteson asymmetric homologation reaction.

机构信息

School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT, UK.

Cornea Research Chair, Department of Optometry, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh 11433, Saudi Arabia.

出版信息

Org Biomol Chem. 2021 May 19;19(19):4279-4284. doi: 10.1039/d1ob00604e.

Abstract

Studies of a catalytic asymmetric version of the Matteson reaction between dichloromethylboronates and organolithium reagents have been undertaken. From several different chiral catalytic systems studied, only one based on a mannitol derivative has given substantial asymmetric induction close to that previously achieved with a bis(oxazoline) derivative and ytterbium triflate. More detailed study of the latter reaction revealed that fresh ytterbium triflate actually reduced the level of asymmetric induction, while "aged" ytterbium triflate, or a fresh sample that had been treated with water, brought about improved induction. The implications of these findings are discussed.

摘要

已经进行了手性催化不对称版本的 Matteson 反应的研究,该反应是二氯甲基硼酸酯和有机锂试剂之间的反应。在所研究的几种不同的手性催化体系中,只有一种基于甘露醇衍生物的体系给出了与以前使用双恶唑啉衍生物和 ytterbium triflate 接近的大的不对称诱导。对后一种反应的更详细研究表明,新鲜的 ytterbium triflate 实际上降低了不对称诱导的水平,而“老化”的 ytterbium triflate 或经过水处理的新鲜样品则带来了改善的诱导。讨论了这些发现的意义。

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