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A surprising switch in absolute configuration of anti-inflammatory macrolactones. Johannes Tauber, Markus Rohr, Thorsten Walter, Dieter Schollmeyer, Karin Rahn-Hotze, Gerhard Erkel, Till Opatz , Org. Biomol. Chem. , 2016 , 14 , 3695

Sumalactones A–D, four new curvularin-type macrolides from a marine deep sea fungus Penicillium Sumatrense. Yue-Hua Wu, Zhi-Han Zhang, Yue Zhong, Jun-Jun Huang, Xiao-Xia Li, Jin-Yan Jiang, Yin-Yue Deng, Lian-Hui Zhang, Fei He , RSC Adv. , 2017 , 7 , 40015

828. Curvularin. Part I. Isolation and partial characterisation of a metabolic product from a new species of Curvularia. O. C. Musgrave , J. Chem. Soc. , 1956 , 4301

638. Studies in relation to biosynthesis. Part XX. The structure and biosynthesis of curvularin. A. J. Birch, O. C. Musgrave, R. W. Rickards, Herchel Smith , J. Chem. Soc. , 1959 , 3146

Curvularin. Part V. The compound C16H18O5, αβ-dehydrocurvularin. H. D. Munro, O. C. Musgrave, Richard Templeton , J. Chem. Soc. C , 1967 , 947

218. Curvularin. Part II. The constitution of an aromatic degradation product and the partial structure of curvularin. O. C. Musgrave , J. Chem. Soc. , 1957 , 1104

Stereodivergent routes in organic synthesis: marine natural products, lactones, other natural products, heterocycles and unnatural compounds. Carmen Nájera, Francisco Foubelo, José M. Sansano, Miguel Yus , Org. Biomol. Chem. , 2020 , 18 , 1279

Selective inhibition of p97 by chlorinated analogues of dehydrocurvularin. Joseph Tillotson, Bharat P. Bashyal, MinJin Kang, Taoda Shi, Fabian De La Cruz, A. A. Leslie Gunatilaka, Eli Chapman , Org. Biomol. Chem. , 2016 , 14 , 5918

Bioactive natural products derived from mangrove-associated microbes. Jing Xu , RSC Adv. , 2015 , 5 , 841

41. Curvularin. Part IV. Synthesis of a degradation product. A. J. Birch, B. Moore, R. W. Rickards , J. Chem. Soc. , 1962 , 220