Marine Drugs Research Center, College of Pharmacy, Jinan University , 601 Huangpu Avenue West, Guangzhou 510632, P. R. China.
Institute of Organic Chemistry, University of Würzburg , Am Hubland, Würzburg D-97074, Germany.
Org Lett. 2017 Jan 6;19(1):182-185. doi: 10.1021/acs.orglett.6b03479. Epub 2016 Dec 19.
Krishnadimer A (1a), a C-symmetric limonoid dimer representing a new class of axially chiral nonbiaryl natural products, was isolated and biomimetically semisynthesized by atroposelective 2,3-dichloro-5,6-dicyanobenzoquinone-mediated dienol-oxidative coupling. Single-crystal X-ray diffraction and electronic circular dichroism spectral analysis on the synthesized 1a unambiguously established its absolute configuration, including the P-configuration of the C15-C15' central axis. Antitumor investigations of the synthesized dimers 1a, 2a, and 2b revealed the large impact of axial chirality on bioactivities.
Krishnadimer A (1a) 是一种 C 对称的柠檬素二聚体,代表了一类新的轴向手性非联芳烃天然产物,它通过对映选择性的 2,3-二氯-5,6-二氰基苯醌介导的二烯醇-氧化偶联反应被分离并仿生半合成。对合成的 1a 进行单晶 X 射线衍射和电子圆二色光谱分析,明确确定了其绝对构型,包括 C15-C15' 中心轴的 P 构型。对合成的二聚体 1a、2a 和 2b 的抗肿瘤研究表明,轴向手性对生物活性有很大影响。