Suppr超能文献

具有强给电子取代基的 1,2-二硼烷:合成与高抗菌活性。

1,2-Diborolanes with strong donor substituents: Synthesis and high antimicrobial activity.

机构信息

Department of Chemistry, Faculty of Arts and Sciences, Adnan Menderes University, 09010 Aydın, Turkey.

Department of Physics, Faculty of Science, Dokuz Eylül University, 35160 İzmir, Turkey.

出版信息

Bioorg Chem. 2021 Jan;106:104494. doi: 10.1016/j.bioorg.2020.104494. Epub 2020 Nov 21.

Abstract

1,2-diborolanes with strong and without strong donor substituents have been described, and are also referred to as 1,2-diboracyclopentane. The 1,2-diaryl/alkyl-amino-1,2-diboracyclopentanes 2, 3, and 4 were obtained in good yield after the reaction of 1,2-dichloro-1,2-diboracyclopentane 1 with ArNHLi and MeSi-NR. The structures of these new derivatives were characterized by nuclear magnetic resonance spectroscopy. The molecular structures of 2b, 2c, 2e, 4, and 5f were also determined by single-crystal X-ray diffraction. The newly synthesized 1,2-borolanes are stable in air and showed particularly high activity against some Gram-positive bacteria.

摘要

1,2-二硼烷具有强给体和无强给体取代基,也被称为 1,2-二硼杂环戊烷。1,2-二氯-1,2-二硼杂环戊烷 1 与 ArNHLi 和 MeSi-NR 反应后,得到了收率较高的 1,2-二芳基/烷基-氨基-1,2-二硼杂环戊烷 2,3 和 4。这些新衍生物的结构通过核磁共振波谱进行了表征。2b、2c、2e、4 和 5f 的单晶 X 射线衍射也确定了它们的分子结构。新合成的 1,2-硼烷在空气中稳定,对一些革兰氏阳性菌表现出特别高的活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验