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Volumn 22, Issue 18, 1981, Pages 1705-1708

A new synthetic method: Direct replacement of the nitro group by hydrogen or deuterium

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Indexed keywords


EID: 0001010494     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)90417-4     Document Type: Article
Times cited : (152)

References (12)
  • 6
    • 0001094805 scopus 로고
    • 1-Benzyl-1,4-dihydronicotinamide as a reagent for replacing aliphatic nitro groups by hydrogen: an electron-transfer chain reaction
    • 3SNa may occur in preference to the reduction. Similarly, method B is not suitable for these compounds owing to its strong basicity of the reagent. The reagent of method C is not nucleophilic nor basic, but lacks reactivity. The compounds of entry 1, 2, 4, 5, 6, 7, 9, 10, 11, 12, 16 can not be reduced by this method. In these regards the method reported here is the best one known to date for replacing the nitro group by hydrogen.
    • (1980) Journal of the American Chemical Society , vol.102 , pp. 2581
    • Ono1    Tamura2    Kaji3
  • 7
    • 84914354179 scopus 로고    scopus 로고
    • 3SnONO.
  • 12
    • 84914354178 scopus 로고    scopus 로고
    • Acylation of the nitro compounds can be done by the following reactions


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.