Affiliation:
1. School of Chemistry and Chemical Engineering
2. Chongqing University
3. Chongqing
4. P. R. China
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Chongqing Basic and Frontier Research Project
Venture and Innovation Support Program for Chongqing Overseas Returnees
Publisher
Royal Society of Chemistry (RSC)
Cited by
11 articles.
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1. Synthesis of γ-Thiapyrones by Diels–Alder/Retro-Diels–Alder Reaction of α-Pyrones with 5-H-1,2,3-Thiadiazoles;The Journal of Organic Chemistry;2024-04-08
2. 1,2,3-Thiadiazole as a Modifiable and Scalable Directing Group for ortho-C–H Functionalization;Organic Letters;2024-02-15
3. Recent Advances in the Denitrogenative Annulation Reactions of 1,2,3‐Thiadiazoles;ChemCatChem;2024-02-13
4. Regioselectivity for the Rh(I)‐catalyzed Annulation of 1,2,3‐Thiadiazoles with Alkynes: Experimental and Computational Analysis Reveal the Surprising Role of the Alkyne Substituent;ChemCatChem;2023-11-20
5. The effect of the C5-substituent on regioselectivity in the Rh(i)-catalyzed intermolecular transannulation of 1,2,3-thiadiazoles with phenylacetylene;Catalysis Science & Technology;2023