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Supporting Information File 1: Experimental procedures and NMR spectra of all newly synthesized compounds. | ||
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Cite the Following Article
Asymmetric synthesis of a highly functionalized bicyclo[3.2.2]nonene derivative
Toshiki Tabuchi, Daisuke Urabe and Masayuki Inoue
Beilstein J. Org. Chem. 2013, 9, 655–663.
https://doi.org/10.3762/bjoc.9.74
How to Cite
Tabuchi, T.; Urabe, D.; Inoue, M. Beilstein J. Org. Chem. 2013, 9, 655–663. doi:10.3762/bjoc.9.74
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- Hagiwara, K.; Urabe, D.; Inoue, M. Studies in symmetry-driven synthesis of ryanodol: application of nucleophilic alkynylation for regio- and stereoselective desymmetrization. Tetrahedron Letters 2014, 55, 3817–3819. doi:10.1016/j.tetlet.2014.05.075
- Nagatomo, M.; Koshimizu, M.; Masuda, K.; Tabuchi, T.; Urabe, D.; Inoue, M. Total synthesis of ryanodol. Journal of the American Chemical Society 2014, 136, 5916–5919. doi:10.1021/ja502770n