Correction: Tallarita et al. The Role of –OEt Substituents in Molybdenum-Assisted Pentathiepine Formation—Access to Diversely Functionalized Azines. Molecules 2024, 29, 3806
Roberto Tallarita, Lukas M. Jacobsen, Siva S. M. Bandaru, Benedict J. Elvers, Carola Schulzke
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsAdvanced Synthetic Organic Chemistry · Coordination Chemistry and Organometallics · Asymmetric Hydrogenation and Catalysis
Supplemental Materials
In the original publication [1], the Supplementary Materials file was submitted but could not be accessed for technical reasons. As part of this correction, the authors are including Figure S61, which demonstrates that precursor 4g (data from the original publication) is a tautomer.
The Corrected Supplementary Materials should be read as follows:
- Supplementary Materials: The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules29163806/s1, Figures S1–S38: ^1^H, ^13^C NMR spectra of 3a, 3c, 4’a, 3d, 6, 4b, 4c, 4d, 2d, 8, 4e, 4f, 4g, 5c, 5d, 5e, 5f, 13, 14. Figures S39–S42: UV-vis spectra of 5c, 5d, 5e, 5f. Figures S43–S60: APCI Mass spectra of 3a, 3c, 4c, 4g, 4b, 4’a, 2d, 3d, 4d, 13, 14, 8, 4e, 4f, 5c, 5d, 5e, 5f. Figure S61: Tautomerism of precursor 4g (2-(3-ethoxybuta-1,2-dien-1-yl)pyridine to the left and 2-(3-ethoxybuta-1,3-dien-1-yl)pyridine to the right). Tables S1–S6: Crystal data and structure refinement for 3a, 12, 5c, 5d, 5e, 5f.
The authors state that the scientific conclusions are unaffected by the issue. This correction was approved by the Academic Editor. The original publication has also been updated.
The reference list from the paper itself. Each links out to its DOI / PubMed record.