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Volumn 356, Issue 5, 2014, Pages 946-950

Copper-catalyzed oxidative transformation of secondary alcohols to 1,5-disubstituted tetrazoles

Author keywords

alcohols; azides; copper; regioselectivity; tetrazoles

Indexed keywords


EID: 84897022537     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201300863     Document Type: Article
Times cited : (13)

References (50)
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    • During the revision of this manuscript, Echavarran and co-workers reported a gold-catalyzed synthesis of tetrazoles. See:, M. Gaydou, A. M. Echavarren, Angew. Chem. 2013, 125, 13710-13713
    • (2013) Angew. Chem. , vol.125 , pp. 13710-13713
    • Gaydou, M.1    Echavarren, A.M.2
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    • Angew. Chem. Int. Ed. 2011, 50, 11487-11491. The reaction of 1a under Jiao's conditions did not furnish the tetrazole 2a, and resulted in the formation of the corresponding chalcone (1,3-diphenyl-2-propen-1-one) (see entry 19, Table 1).
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    • While we were preparing this manuscript Jiao and co-workers reported a silver-catalyzed nitrogenation of alkynes to access tetrazoles. See:, T. Shen, T. Wang, C. quin, N. Jiao, Angew. Chem. 2013, 125, 6809-6812
    • (2013) Angew. Chem. , vol.125 , pp. 6809-6812
    • Shen, T.1    Wang, T.2    Quin, C.3    Jiao, N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.