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Englerina woodfordioides (Schweinf.) Balle — Habit: Shrub. Habitat: LMWF, LMDF; 1 300–3 100 m. Distribution: II. Voucher: Sirimon Track, Alt. 2 667 m, 17 Jul. 2014, CPG 28338 (EA). References: Bussmann (1993, 1994), Bussmann & Beck (1995a), Polhill & Wiens (1999a), Agnew (2013)., Published as part of Zhou, Ya-Dong, Mwachala, Geoffrey, Hu, Guang-Wan & Wang, Qing-Feng, 2022, Annotated checklist of the vascular plants of Mount Kenya, East Africa, pp. 1-108 in Phytotaxa 546 (1) on page 66, DOI: 10.11646/phytotaxa.546.1.1, http://zenodo.org/record/6550464, {"references":["Bussmann, R. W. (1993) The forest of Mt. Kenya (Kenya): A phytosociological approach with special reference to ecological problems. Ph. D. Thesis, Eberhard Karls Universitat Tubingen, Tubingen, 119 pp.","Bussmann, R. W. (1994) The forest of Mt. Kenya (Kenya): Vegetation, ecology, destruction and management of a tropical mountain forest ecosystem. Ph. D. dissertation, Universitat Bayreuth Startseite, Bayreuth, 252 pp.","Bussmann, R. W. & Beck, E. (1995 a) The forests of Mt. Kenya (Kenya), a phytosociological synopsis. Phytocoenologia 25 (4): 467 - 560. https: // doi. org / 10.1127 / phyto / 25 / 1995 / 467","Polhill, R. M. & Wiens, D. (1999 a) Loranthaceae. In: Beentje, H. J. & Whitehouse, C. M. (Eds.) Flora of Tropical East Africa. A. A. Balkema, Rotterdam, 121 pp.","Agnew, A. D. Q. (2013) Upland Kenya wild flowers and ferns, 3 rd edn. Nature Kenya Publications, Nairobi, 733 pp."]}

We report the synthesis and biological evaluation of a series of (−)‐englerin A analogues obtained along our previously reported synthetic route based on a stereoselective gold(I) cycloaddition process. This synthetic route is a convenient platform to access analogues with broad structural diversity and has led us to the discovery of unprecedented and easier‐to‐synthesize derivatives with an unsaturation in the cyclopentyl ring between C4 and C5. We also introduce novel analogues in which the original isopropyl motif has been substituted with cyclohexyl, phenyl, and cyclopropyl moieties. The high selectivity and growth‐inhibitory activity shown by these new derivatives in renal cancer cell lines opens new ways toward the final goal of finding effective drugs for the treatment of renal cell carcinoma (RCC).