(+)- and (−)-actinoxocine, and actinaphthorans A–B, C-ring expansion and cleavage angucyclinones from a marine-derived Streptomyces sp.

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发布日期 2019-10-23

DOI 10.1039/C9QO01154D

影响因子 5.281

作者

Shumin Zhang, Lu Zhang, Xinzhen Fu, Zhi Li, Lin Guo, Lijuan Kou, Ming Liu, Zeping Xie

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摘要

(+)- and (−)-actinoxocine (1), a pair of enantiomeric C-ring expansion angucyclinones, featuring a unique epoxybenzo[f]naphtho[1,8-bc]oxocine carbon skeleton, and two unusual C-ring cleavage analogues, actinaphthorans A–B (2–3), were isolated from a marine-derived Streptomyces sp. Their structures and absolute configurations were assigned by spectroscopic analysis, X-ray diffraction and CD calculations.

期刊推荐

Acta Materialia

Journal of Natural Medicines

Chemistry Education Research and Practice

Organic Process Research & Development

Russian Chemical Bulletin

Journal of Saudi Chemical Society

Russian Journal of Coordination Chemistry

Russian Journal of Bioorganic Chemistry

New Journal of Chemistry

Saudi Pharmaceutical Journal

来源期刊

Organic Chemistry Frontiers

CiteScore: 7.8

自引率: 8.7%

年发文量: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

(+)- and (−)-actinoxocine, and actinaphthorans A–B, C-ring expansion and cleavage angucyclinones from a marine-derived Streptomyces sp.

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