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Volumn 46, Issue 17, 2005, Pages 3079-3083

General-buffer catalysis of the reaction of N-(hydroxymethyl)benzamide: A new pathway for the aqueous reaction of carbinolamides

Author keywords

Buffer catalysis; Carbinolamide; N (Hydroxymethyl)benzamide

Indexed keywords

ACETIC ACID; AMIDE; BENZAMIDE DERIVATIVE; BUFFER; CHLOROACETIC ACID; DICHLOROACETIC ACID; N (HYDROXYMETHYL)BENZAMIDE; PIVALIC ACID; UNCLASSIFIED DRUG;

EID: 15944406493     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.03.011     Document Type: Article
Times cited : (9)

References (46)
  • 15
    • 0004255131 scopus 로고
    • H. Bundgaard Elsevier Amsterdam
    • H. Bundgaard H. Bundgaard Design of Prodrugs 1985 Elsevier Amsterdam 1 92
    • (1985) Design of Prodrugs , pp. 1-92
    • Bundgaard, H.1
  • 32
    • 85030807403 scopus 로고    scopus 로고
    • note
    • Solvent system used to separate 1 from 2 via HPLC was 90% 70/30 water/methanol and 10% methanol. The chromatograms were generated by following the reactions at 254 nm
  • 33
    • 85030811470 scopus 로고    scopus 로고
    • note
    • Acetic acid studies were performed at three different pH's while those performed in the presence of dichloroacetic acid and pivalic acid were investigated at only one pH
  • 34
    • 85030814935 scopus 로고    scopus 로고
    • note
    • -1/55.5 M)
  • 35
    • 85030808725 scopus 로고    scopus 로고
    • note
    • The half-life of the water-catalyzed reaction is ∼13 years
  • 37
    • 85030814054 scopus 로고    scopus 로고
    • Arguments for protonation on oxygen or nitrogen could be made based on acid-catalyzed amide hydrolysis studies (see Ref. 20)
    • Arguments for protonation on oxygen or nitrogen could be made based on acid-catalyzed amide hydrolysis studies (see Ref. 20)
  • 45
    • 85030812746 scopus 로고    scopus 로고
    • note
    • a of protonated formaldehyde should be ∼-1.74


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.