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- Profiling patterns of glutathione reductase inhibition by the natural product
illudin S and its acylfulvene analogues. Xiaodan Liu, Shana J. Sturla
, Mol. BioSyst.
, 2009
, 5
, 1013
- Fluorescent constituents and cultivation of Lampteromyces japonicus. M. Endo, M. Kajiwara, K. Nakanishi
, J. Chem. Soc. D
, 1970
, 309
- Secondary mould metabolites. Part 59.1
Sesquiterpene illudanes: semi-synthesis of new illudins, structures and biological activity. Alberto Arnone, Lucio Merlini, Gianluca Nasini, Orso Vajna de Pava, Franco Zunino
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 610
- The absolute configuration of illudin S; application of the dibenzoate chirality rule. N. Harada, K. Nakanishi
, J. Chem. Soc. D
, 1970
, 310
- Fungi bioluminescence revisited. Dennis E. Desjardin, Anderson G. Oliveira, Cassius V. Stevani
, Photochem. Photobiol. Sci.
, 2008
, 7
, 170
- Total synthesis of hydroxymethylacylfulvene, an antitumour
derivative of illudin S. Trevor C. McMorris, Yi Hu, Jian Yu, Michael J. Kelner
, Chem. Commun.
, 1997
, 315
- Studies in terpenoid biosynthesis. Part 26. Applications of 2H and 13C n.m.r. spectroscopy to the biosynthesis of the illudin sesquiterpenoids. A. Peter W. Bradshaw, James R. Hanson, Ian H. Sadler
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 2445
- Application of Pauson–Khand reaction in the total synthesis of terpenes. Majid M. Heravi, Leila Mohammadi
, RSC Adv.
, 2021
, 11
, 38325
- Non-peptide secondary metabolites from poisonous mushrooms: overview of chemistry, bioactivity, and biosynthesis. Seulah Lee, Jae Sik Yu, Seoung Rak Lee, Ki Hyun Kim
, Nat. Prod. Rep.
, 2022
, 39
, 512
- Biosynthesis of illudosin, a fomannosane-type sesquiterpene, by the Basidiomycete Omphalotus nidiformis. Maree L. Burgess, Kevin D. Barrow
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 2461