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Volumn 80, Issue 1, 2010, Pages 177-181

Preparation of 2-sulfonyl-1,2,3-triazoles by base-promoted 1,2-rearrangement of a sulfonyl group

Author keywords

1,2,3 Triazole; Base Promoted Reaction; Rearrangement; Regioselective Reaction; Sulfonyl Group

Indexed keywords


EID: 76949104154     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-09-S(S)44     Document Type: Article
Times cited : (27)

References (29)
  • 16
    • 57349191194 scopus 로고    scopus 로고
    • 2 afforded a mixture of 1-tosyl and 2-tosyl triazoles (80%, l-tosyl:2-tosyl = 82:18). See also
    • 2 afforded a mixture of 1-tosyl and 2-tosyl triazoles (80%, l-tosyl:2-tosyl = 82:18). See also. Horneff T., Chuprakov S., Chernyak N., Gevorgyan V., and Fokin V.V. J. Am. Chem. Soc. 130 (2008) 14972
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14972
    • Horneff, T.1    Chuprakov, S.2    Chernyak, N.3    Gevorgyan, V.4    Fokin, V.V.5
  • 23
    • 0002884076 scopus 로고
    • For sulfonyl group rearrangement of other heterocycles, see
    • For sulfonyl group rearrangement of other heterocycles, see. Kohori K., Kinoshita H., and Inomata K. Chem. Lett. (1995) 799
    • (1995) Chem. Lett. , pp. 799
    • Kohori, K.1    Kinoshita, H.2    Inomata, K.3
  • 27
    • 76949097994 scopus 로고    scopus 로고
    • note
    • 2 were also effective for the rearrangement of sulfonyl group.
  • 28
    • 76949093002 scopus 로고    scopus 로고
    • note
    • + 300.0807. Found m/z 300.0801.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.