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来自石松生异丝壳菌的三联苯衍生物。

Terphenyl Derivatives from Allantophomopsis lycopodina.

作者信息

Andernach Lars, Sandjo Louis P, Liermann Johannes C, Schlämann Ricardo, Richter Christian, Ferner Jan-Peter, Schwalbe Harald, Schüffler Anja, Thines Eckhard, Opatz Till

机构信息

Institute of Organic Chemistry, Johannes Gutenberg-University , Duesbergweg 10-14, D-55128 Mainz, Germany.

Departamento de Ciências Farmacêuticas, Centro de Ciências da Saúde, Bloco J/K, Universidade Federal de Santa Catarina , Florianópolis 88040-900, SC, Brazil.

出版信息

J Nat Prod. 2016 Oct 28;79(10):2718-2725. doi: 10.1021/acs.jnatprod.6b00690. Epub 2016 Oct 12.

Abstract

Three secondary fungal metabolites 1-3 with a benzo[b]naphtho[2,1-d]furan skeleton were isolated from submerged cultures of the ascomycete Allantophomopsis lycopodina. The NMR-based structure elucidation was challenging due to a low H/C ratio of only 0.64 and 0.68, respectively. NMR measurements in two different solvents and the use of NMR experiments such as HSQC-TOCSY and LR-HSQMBC proved to be helpful in this respect. The proposed structures obtained from the comprehensive analysis of the NMR data were verified by comparison of recorded and computed NMR chemical shifts from quantum chemical calculations of several constitutional isomers and were further analyzed with the aid of the DP4 and DP4+ probabilities.

摘要

从子囊菌纲的石松拟盘多毛孢(Allantophomopsis lycopodina)的深层培养物中分离出三种具有苯并[b]萘并[2,1-d]呋喃骨架的次生真菌代谢产物1-3。基于核磁共振(NMR)的结构解析具有挑战性,因为它们的氢碳比(H/C)分别仅为0.64和0.68。在两种不同溶剂中进行的核磁共振测量以及使用诸如HSQC-TOCSY和LR-HSQMBC等核磁共振实验在这方面被证明是有帮助的。通过比较从几种构造异构体的量子化学计算中记录的和计算的核磁共振化学位移,验证了从核磁共振数据的综合分析中获得的所提出的结构,并借助DP4和DP4+概率进行了进一步分析。

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