Cycloprop-2-ene-1-carboxylates: Potential chemical biology tools in the early growth stage of <i>Arabidopsis thaliana</i>
Author:
Affiliation:
1. Graduate School of Agricultural and Life Sciences, The University of Tokyo
Publisher
Pesticide Science Society of Japan
Subject
Health, Toxicology and Mutagenesis,Insect Science
Link
https://www.jstage.jst.go.jp/article/jpestics/48/2/48_D22-034/_pdf
Reference18 articles.
1. 1) B. Prasad Raiguru, S. Nayak, D. Ranjan Mishra, T. Das, S. Mohapatra and N. Priyadarsini Mishra: Synthetic applications of cyclopropene and cyclopropenone: Recent progress and developments. Asian J. Org. Chem. 9, 1088–1132 (2020).
2. 2) A. Greenberg, R. P. T. Tomkins, M. Dobrovolny and J. F. Liebman: The strain energy of diphenylcyclopropenone: A reexamination. J. Am. Chem. Soc. 105, 6855–6858 (1983).
3. 3) Z. Yu, Y. Pan, Z. Wang, J. Wang and Q. Lin: Genetically encoded cyclopropene directs rapid, photoclick-chemistry-mediated protein labeling in mammalian cells. Angew. Chem. Int. Ed. 51, 10600–10604 (2012).
4. 4) G. Triola, G. Fabriàs and A. Llebaria: Synthesis of a cyclopropene analogue of ceramide, a potent inhibitor of dihydroceramide desaturase. Angew. Chem. Int. Ed. 40, 1960–1962 (2001).
5. 5) D. M. Patterson, K. A. Jones and J. A. Prescher: Improved cyclopropene reporters for probing protein glycosylation. Mol. Biosyst. 10, 1693–1697 (2014).
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