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Volumn , Issue 3, 2004, Pages 614-622

Nitrosation of Amines in Non-Aqueous Solvents - Difference between N-N=O and O-N=O Nitroso Donors

Author keywords

Kinetics; Mechanism; Nitrosation; Solvent effect; Sulfonamide

Indexed keywords

1 METHYLPIPERAZINE; 18 CROWN 6; AMINE; CROWN ETHER; CYCLOHEXANE; ISOPROPYLAMINE; MORPHOLINE; N METHYL N NITROSOBENZENESULFONAMIDE; N NITROSOSULFONAMIDE DERIVATIVE; NITRITE; NITROGEN; NITROSO DERIVATIVE; OXYGEN; PIPERAZINE DERIVATIVE; PIPERIDINE DERIVATIVE; PROPYLAMINE; PYRROLIDINE DERIVATIVE; SOLVENT; SULFONAMIDE; UNCLASSIFIED DRUG;

EID: 1242263414     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300482     Document Type: Article
Times cited : (8)

References (26)
  • 11
    • 0004206788 scopus 로고
    • Cambridge University Press Cambridge
    • D. L. H. Williams, Nitrosation; Cambridge University Press: Cambridge, 1988.
    • (1988) Nitrosation
    • Williams, D.L.H.1
  • 24
    • 1242316789 scopus 로고    scopus 로고
    • note
    • -3.
  • 26
    • 1242271836 scopus 로고    scopus 로고
    • note
    • -1 is obtained for the six-membered transition state. We think that the temperature study showing Arrhenius behavior - in contrast with that observed in the amine nitrosation by alkyl nitrites - is important.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.