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通过过渡金属催化的 B-H 活化合成多面体硼烷簇杂环。

Synthesis of Polyhedral Borane Cluster Fused Heterocycles via Transition Metal Catalyzed B-H Activation.

机构信息

State Key Laboratory of Environment-Friendly Energy Materials & School of Material Science and Engineering, Southwest University of Science and Technology, 59 Qinglong Road, Mianyang 621010, Sichuan, China.

出版信息

Molecules. 2020 Jan 17;25(2):391. doi: 10.3390/molecules25020391.

Abstract

Aromatic heterocycles are ubiquitous building blocks in bioactive natural products, pharmaceutical and agrochemical industries. Accordingly, the carborane-fused heterocycles would be potential candidates in drug discovery, nanomaterials, metallacarboranes, as well as photoluminescent materials. In recent years, the transition metal catalyzed B-H activation has been proved to be an effective protocol for selective functionalization of B-H bond of -carboranes, which has been further extended for the synthesis of polyhedral borane cluster-fused heterocycles via cascade B-H functionalization/annulation process. This article summarizes the recent progress in construction of polyhedral borane cluster-fused heterocycles via B-H activation.

摘要

芳杂环是生物活性天然产物、医药和农用化学品工业中无处不在的构建模块。相应地,笼型硼烷杂环将是药物发现、纳米材料、金属笼型硼烷以及光致发光材料中的潜在候选物。近年来,过渡金属催化的 B-H 活化已被证明是 -carboranes 的 B-H 键选择性功能化的有效方法,该方法已进一步扩展,通过级联 B-H 功能化/环化反应合成多面体硼烷簇杂环。本文总结了通过 B-H 活化构建多面体硼烷杂环的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e344/7024252/39a9f01e0744/molecules-25-00391-sch001.jpg

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