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Thiemann, T., Noltemeyer, M. and De Meijere, A. (1997) Chiral Building Blocks from ( )-(S)-7,7a-Dihydro-7a-Methylindane-1,5(6H)-Dione (Hajos-Parrish Diketone). Reports of the Institute of Advanced Material Study, Kyushu University, 11, 147-152.
https://catalog.lib.kyushu-u.ac.jp/opac_download_md/7880/KJ00004507847.pdf

has been cited by the following article:

• TITLE: Steroids, Tri- and Meroterpenoids with a Quinone Structure—A Review

  AUTHORS: Maryam S. M. Aghaei, Thies Thiemann

  KEYWORDS: Steroid, Secosteroid, Meroterpenoid, Triterpenoid, Quinone, Anti-Tumour Agent, Antibiotic, Natural Product

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.14 No.1, March 29, 2024

  ABSTRACT: Terpenoids with quinoid structures are found as natural products. This includes steroidal quinones, quinones with a secosteroid structure and meroterpenoid quinones. Importantly, catechol estrogens as endogenous metabolites of estradiol and estrone are precursors of reactive quinones and semiquinones, which are thought to contribute to estrogen-induced carcinogenesis. On the other hand, a number of quinones that include substituted naphthoquinones and anthraquinones are highly cytotoxic and have been used in cancer treatment. This makes the structures interesting synthetic targets. The following is a review of important natural and synthetic terpenoid and steroid quinone hybrids.