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- Towards the enantioselective synthesis of (−)-euonyminol – preparation of a fully functionalised lower-rim model. Matthew J. Webber, Sarah A. Warren, Damian M. Grainger, Matthew Weston, Stacy Clark, Steven J. Woodhead, Lyn Powell, Stephen Stokes, Alexander Alanine, Jeffrey P. Stonehouse, Christopher S. Frampton, Andrew J. P. White, Alan C. Spivey
, Org. Biomol. Chem.
, 2013
, 11
, 2514
- Dihydroagarofuran sesquiterpenoid derivatives from the leaves of Tripterygium wilfordii with potential neuroprotective effects against H2O2-induced SH-SY5Y cell injuries. Shu-Hui Dong, Ming Bai, Zi-Lin Hou, Wei-Yu Zhou, Guo-Dong Yao, Bin Lin, Xiao-Xiao Huang, Shao-Jiang Song
, New J. Chem.
, 2020
, 44
, 10258
- Celastraceae sesquiterpene pyridyl ligands. Chen Dai, Alan C. Spivey
, Org. Chem. Front.
, 2023
, 10
, 5296
- Celastraceae sesquiterpenoids: biological activity and synthesis. Alan C. Spivey, Matthew Weston, Steven Woodhead
, Chem. Soc. Rev.
, 2002
, 31
, 43
- The dihydro-β-agarofuran sesquiterpenoids. Jin-Ming Gao, Wen-Jun Wu, Ji-Wen Zhang, Yasuo Konishi
, Nat. Prod. Rep.
, 2007
, 24
, 1153
- Synthetic Studies of Dihydroagarofuran Sesquiterpene: an Improved NBS–THF–H2O System for Stereoselective Construction of Tetrahydrofuran Moiety. Liang Dong Sun, Yong Qiang Tu, Wu Jiong Xia
, J. Chem. Res. (S)
, 1999
, 490
- Structure of two new sesquiterpenoid insect antifeedants from Celastrus rosthornianus. Yong Q. Tu
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 425
- New sesquiterpene esters and alkaloids from Euonymus japonicus: the ‘Ejap’ series. X-Ray molecular structures of Ejap-2, -3, -4, -5, -6, and -10. Zsuzsanna Rózsa, András Perjési, István Pelczer, Gyula Argay, Alajos Kálmán
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1079
- New sesquiterpene esters from Euonymus europaeus and E. latifolius. Zsuzsanna Rózsa, István Pelczer
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1089
- Nine new dihydro-β-agarofuran sesquiterpene polyesters from the leaves of Tripterygium wilfordii. Le Zhou, Ming Bai, Qing-Jun He, Zi-Lin Hou, Li-Wei Lu, Jie Wang, Xiao-Xiao Huang, Bin Lin, Shao-Jiang Song
, New J. Chem.
, 2022
, 46
, 2423