Transition metal- and oxidant-free sulfonylation of 1-sulfonyl-1H-1,2,3-triazoles to enols for the synthesis of sulfonate derivatives-Reference-Cited by-同舟云学术

Transition metal- and oxidant-free sulfonylation of 1-sulfonyl-1H-1,2,3-triazoles to enols for the synthesis of sulfonate derivatives

Published:2019-03-08 Issue:7 Volume:49 Page:959-972
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

He Xinwei¹^ORCID,Wu Yuhao¹,Zuo Youpeng¹,Xie Mengqing¹,Li Ruxue¹,Shang Yongjia¹^ORCID

Affiliation:

1. Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials (State Key Laboratory Cultivation Base), College of Chemistry and Materials Science, Anhui Normal University, Wuhu, P.R. China

Funder

National Natural Science Foundation of China

Anhui Provincial Natural Science Foundation

Natural Science Foundation of Education Administration of Anhui Province

Special and Excellent Research Fund of Anhui Normal University

Doctoral Scientific Research Foundation of Anhui Normal University

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2019.1582065

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3. Racemization-Free Chemoenzymatic Peptide Synthesis Enabled by the Ruthenium-Catalyzed Synthesis of Peptide Enol EstersviaAlkyne-Addition and Subsequent Conversion Using Alcalase-Cross-Linked Enzyme Aggregates

4. Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters

5. Synthesis of isophthalates from methyl coumalate

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