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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
- Characterization of a reductively-activated elimination pathway relevant to the biological chemistry of the kinamycins and lomaiviticins. Seann P. Mulcahy, Christina M. Woo, Weidong Ding, George A. Ellestad, Seth B. Herzon
, Chem. Sci.
, 2012
, 3
, 1070
- 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
- Total synthesis of hydroxymethylacylfulvene, an antitumour
derivative of illudin S. Trevor C. McMorris, Yi Hu, Jian Yu, Michael J. Kelner
, Chem. Commun.
, 1997
, 315
- Recent advances in the use of temporary silicon tethers in metal-mediated reactions. Sonia Bracegirdle, Edward A. Anderson
, Chem. Soc. Rev.
, 2010
, 39
, 4114
- Electrophilic natural products and their biological targets. Malte Gersch, Johannes Kreuzer, Stephan A. Sieber
, Nat. Prod. Rep.
, 2012
, 29
, 659
- Application of Pauson–Khand reaction in the total synthesis of terpenes. Majid M. Heravi, Leila Mohammadi
, RSC Adv.
, 2021
, 11
, 38325
- Synthesis of functionalized fulvenes: [3 + 2] annulation of ethyl α-chlorocyclopropaneformates with 1,3-dicarbonyl compounds. Yuequan Zhu, Min Zhang, Hongling Yuan, Yuefa Gong
, Org. Biomol. Chem.
, 2014
, 12
, 8828
- Rearrangement of a carboxy-substituted spiro[4.4]nonatriene to annulated fulvenes through a Pd(ii)-mediated 1,5-vinyl shift. Karan Goyal, Garrett A. Kukier, Xiangyang Chen, Aneta Turlik, K. N. Houk, Richmond Sarpong
, Chem. Sci.
, 2023
, 14
, 11809
- Natural sesquiterpenoids. Braulio M. Fraga
, Nat. Prod. Rep.
, 2010
, 27
, 1681