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Synthesis and biological evaluation of potential substrates for the
isolation of the strigol receptor
. Jan Willem J. F. Thuring, Rolf Keltjens, Gerard H. L. Nefkens, Binne Zwanenburg
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 759
- Synthesis and bioactivity of labelled germination stimulants for the isolation and identification of the strigolactone receptor. Anat Reizelman, Suzanne C. M. Wigchert, Cinzia del-Bianco, Binne Zwanenburg
, Org. Biomol. Chem.
, 2003
, 1
, 950
- Strigolactones in chemical ecology: waste products or vital allelochemicals?. Andrew J. Humphrey, Aimee M. Galster, Michael H. Beale
, Nat. Prod. Rep.
, 2006
, 23
, 592
- Synthesis of highly enantio-enriched stereoisomers of hydroxy-GR24. J. C. Morris, C. S. P. McErlean
, Org. Biomol. Chem.
, 2016
, 14
, 1236
- Recent advances in the synthesis of analogues of phytohormones strigolactones with ring-closing metathesis as a key step. Chiara Lombardi, Emma Artuso, Eleonora Grandi, Marco Lolli, Francesca Spirakys, Emanuele Priola, Cristina Prandi
, Org. Biomol. Chem.
, 2017
, 15
, 8218
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Synthesis and biological evaluation of strigol analogues modified in the
enol ether part
. Jan Willem, J. F. Thuring, Angelique A. M. A. van Gaal, Sander J. Hornes, Margreet M. de Kok, Gerard H. L. Nefkens, Binne Zwanenburg
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 767
- Access to benzene-modified 2nd generation strigolactams and GR24 by merging C–H olefination with decarboxylative Giese cyclization. Yuhua Ge, Xingyue Chen, Yi Dong, Hua-Nan Wang, Yangyan Li, Gang Chen
, Org. Biomol. Chem.
, 2021
, 19
, 7141
- Strigolactones: a plant phytohormone as novel anti-inflammatory agents. Jun-Xia Zheng, Yu-Shui Han, Jin-Cai Wang, Hui Yang, Hao Kong, Kang-Jia Liu, Si-Yu Chen, Yi-Rui Chen, Yi-Qun Chang, Wei-Min Chen, Jia-Liang Guo, Ping-Hua Sun
, Med. Chem. Commun.
, 2018
, 9
, 181
- Enantioselective total synthesis and biological evaluation of (−)-solanacol. L. J. Bromhead, A. R. Norman, K. C. Snowden, B. J. Janssen, C. S. P. McErlean
, Org. Biomol. Chem.
, 2018
, 16
, 5500
- Aromatic A-ring analogues of orobanchol, new germination stimulants for seeds of parasitic weeds. Heetika Malik, Wouter Kohlen, Muhammad Jamil, Floris P. J. T. Rutjes, Binne Zwanenburg
, Org. Biomol. Chem.
, 2011
, 9
, 2286