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Volumn 51, Issue 2, 2010, Pages 435-438

Hg cathode-free electrochemical detosylation of N,N-disubstituted p-toluenesulfonamides: mild, efficient, and selective removal of N-tosyl group

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; BENZENESULFONAMIDE DERIVATIVE; BROMOBENZENESULFONAMIDE; MAGNESIUM; MERCURY; N,N DIHEXYLTOSYLAMIDE; PLATINUM; POLYCYCLIC AROMATIC HYDROCARBON; SULFONAMIDE; UNCLASSIFIED DRUG;

EID: 71049142221     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.11.056     Document Type: Article
Times cited : (52)

References (84)
  • 63
    • 71049128147 scopus 로고    scopus 로고
    • Lund H., and Hammerich O. (Eds), Marcel Dekker, New York and references cited therein
    • Lund H. In: Lund H., and Hammerich O. (Eds). Organic Electrochemistry, Fourth Edition, Revised and Expanded. Clearvage and Deprotection (2001), Marcel Dekker, New York 969 and references cited therein
    • (2001) Clearvage and Deprotection , pp. 969
    • Lund, H.1
  • 79
    • 71049129273 scopus 로고    scopus 로고
    • note
    • In the reaction of 3e in DMF, N-formyl-1,2,3,4-tetrahydro-6,7-dimethoxyisoquinoline was obtained in 72% yield. N-Dodecyl-N-methylformamide was also obtained in 52% yield along with 4f in 44% yield when the reaction of 3f was carried out in DMF.
  • 82
    • 71049160338 scopus 로고    scopus 로고
    • note
    • An excess electricity would be used for the reduction of N-H bond of mono-substituted tosylamide moiety in 5 resulting in generation of hydrogen and amide enolates.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.