Synlett 2012; 23(10): 1529-1533
DOI: 10.1055/s-0031-1291042
letter
© Georg Thieme Verlag Stuttgart · New York

Potassium tert-Butoxide Promoted Cycloaddition Reaction for the Synthesis of 1,5-Disubstituted 1,2,3-Triazoles from Aromatic Azides and Trimethylsilyl-Protected Alkynes

Authors

  • Luyong Wu*

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Yuxue Chen

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Mi Tang

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Xinming Song

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Guangying Chen

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Xiaoping Song

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
  • Qiang Lin

    College of Chemistry and Chemical Engineering, Hainan Normal University, No.99, Longkun South Road, Haikou 571158, P. R. of China, Fax: +86(898)65889422.   eMail: wuluyong@hainnu.edu.cn
Weitere Informationen

Publikationsverlauf

Received: 03. Januar 2012

Accepted after revision: 25. März 2012

Publikationsdatum:
25. Mai 2012 (online)


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Abstract

The cycloaddition reaction of aromatic azides and trimethylsilyl alkynes upon treatment with desilylating reagents was investigated. In the process, the use of t-BuOK in wet DMF generated 1,5-disubstituted 1,2,3-triazoles regioselectively in moderate to good yields at ambient temperature.

Supporting Information