Supporting Information
For crystallographic data see also CCDC 1824587 and 1824588.
| Supporting Information File 1: Schemes S1 and S2 on the syntheses of compounds 1, 2, and 3a–g; the NMR study for the structure determinations, further DFT calculations, the ORTEP drawing of both sulfone of 5a, 11d and the 1H and 13C NMR charts. | ||
| Format: PDF | Size: 5.1 MB | Download |
| Supporting Information File 2: Crystallographic information of compound 11d. | ||
| Format: TXT | Size: 39.8 KB | Download |
| Supporting Information File 3: Crystallographic information of the sulfone of compound 5a. | ||
| Format: TXT | Size: 37.2 KB | Download |
Cite the Following Article
Unprecedented nucleophile-promoted 1,7-S or Se shift reactions under Pummerer reaction conditions of 4-alkenyl-3-sulfinylmethylpyrroles
Takashi Go, Akane Morimatsu, Hiroaki Wasada, Genzoh Tanabe, Osamu Muraoka, Yoshiharu Sawada and Mitsuhiro Yoshimatsu
Beilstein J. Org. Chem. 2018, 14, 2722–2729.
https://doi.org/10.3762/bjoc.14.250
How to Cite
Go, T.; Morimatsu, A.; Wasada, H.; Tanabe, G.; Muraoka, O.; Sawada, Y.; Yoshimatsu, M. Beilstein J. Org. Chem. 2018, 14, 2722–2729. doi:10.3762/bjoc.14.250
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