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Volumn 51, Issue 3, 2012, Pages 775-779

Nickel- and cobalt-catalyzed direct alkylation of azoles with N-tosylhydrazones bearing unactivated alkyl groups

Author keywords

alkylation; azoles; C H functionalization; cobalt; nickel

Indexed keywords

1 ,10-PHENANTHROLINE; ALKYL CHAIN; ALKYL GROUPS; AZOLES; BENZOTHIAZOLES; BENZOXAZOLE; C-H FUNCTIONALIZATION; COBALT CATALYST; DIRECT ALKYLATION; NICKEL CATALYSIS;

EID: 84855782107     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106825     Document Type: Article
Times cited : (197)

References (115)
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  • 46
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    • For an alternative approach with alkylboronic acids or alkyltin reagents, see
    • Angew. Chem. Int. Ed. Engl. 1997, 36, 119. For an alternative approach with alkylboronic acids or alkyltin reagents, see
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    • for Friedel-Crafts-type alkylations through π-activation of alkenes, see
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    • Gao, K.1    Yoshikai, N.2
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    • The N-tosylhydrazone was completely consumed because of the instability of the corresponding diazo compound under reaction conditions.
    • R. S. Sánchez, F. A. Zhuravlev, J. Am. Chem. Soc. 2007, 129, 5824. The N-tosylhydrazone was completely consumed because of the instability of the corresponding diazo compound under reaction conditions.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5824
    • Sánchez, R.S.1    Zhuravlev, F.A.2
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    • Ref. [4h] and [7e].
    • N. Yoshikai, Synlett 2011, 1047; and Ref. [4h] and [7e].
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    • The reaction with an in situ generated lithium hydrazide also failed to give the coupling product in a satisfactory yield (see the following scheme).
    • The reaction with an in situ generated lithium hydrazide also failed to give the coupling product in a satisfactory yield (see the following scheme);, G. Kaufman, F. Cook, H. Shechter, J. Bayless, L. Friedman, J. Am. Chem. Soc. 1967, 89, 5736.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 5736
    • Kaufman, G.1    Cook, F.2    Shechter, H.3    Bayless, J.4    Friedman, L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.