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Volumn 2, Issue 4, 2004, Pages 593-600

Hydrolytic reactions of 3′-N-phosphoramidate and 3′-N-thiophosphoramidate analogs of thymidylyl-3′,5′-thymidine

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM COMPOUNDS; CATALYSIS; CHEMICAL BONDS; DESULFURIZATION; GEL PERMEATION CHROMATOGRAPHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; MASS SPECTROMETRY; PH EFFECTS; RATE CONSTANTS; REACTION KINETICS; SILICA GEL; STEREOCHEMISTRY;

EID: 1342281334     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b313470a     Document Type: Article
Times cited : (9)

References (37)
  • 2
    • 77956770649 scopus 로고    scopus 로고
    • J. A. Bristol, Ed., Academic Press, San Diego
    • (b) P. D. Cook, in Annual Reports in Medicinal Chemistry, J. A. Bristol, Ed., Academic Press, San Diego 1998, pp. 313-325;
    • (1998) Annual Reports in Medicinal Chemistry , pp. 313-325
    • Cook, P.D.1
  • 16
    • 1342339508 scopus 로고    scopus 로고
    • note
    • 5 The dephosphorylation of 3′-Unp proceeds by a dissociative mechanism without participation of the 2′-OH group. Accordingly, we propose by analogy that thymidine 3′-N-phosphoramidate 11 would be readily dephosphorylated to 3′-aminothymidine 4, if formed during the hydrolysis of 3 at pH 8. However, it must be noted that 10 may possibly also degrade by some other routes to yield small amounts of free thymine and all the possible reactions cannot be distingushed on the basis of the present data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.