Bioorganic Chemistry ( IF 4.5 ) Pub Date : 2020-11-21 , DOI: 10.1016/j.bioorg.2020.104494 Yüksel Şahin 1 , Esin Poyrazoğlu Çoban 1 , Resul Sevinçek 2 , Hacı Halil Bıyık 1 , Hüseyin Özgener 3 , Muhittin Aygün 2
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 Me3Si-NR2. 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.
中文翻译:
具有强供体取代基的 1,2-二硼烷:合成和高抗菌活性
已经描述了具有强供体取代基和不具有强供体取代基的1,2-二硼烷,并且也被称为1,2-二硼环戊烷。1,2-二芳基/烷基-氨基-1,2- diboracyclopentanes 2,3和4以良好的收率1,2-二氯-1,2-二diboracyclopentane的反应后获得1与ArNHLi和Me 3 SI- NR 2。这些新衍生物的结构通过核磁共振波谱表征。2b , 2c , 2e , 4 , 5f的分子结构还通过单晶 X 射线衍射测定。新合成的 1,2-硼烷在空气中稳定,对某些革兰氏阳性菌表现出特别高的活性。