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Volumn 43, Issue 42, 2002, Pages 7569-7571

Facile synthesis of a selectively protected triazamacrocycle

Author keywords

[No Author keywords available]

Indexed keywords

1,7 DIAMINOHEPTANE; AZIRIDINE DERIVATIVE; MACROCYCLIC COMPOUND; N (2 NITROBENZENESULFONYL)AZIRIDINE; TRIAZAMACROCYCLE; UNCLASSIFIED DRUG;

EID: 0037078355     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01756-2     Document Type: Article
Times cited : (4)

References (15)
  • 5
    • 0000383690 scopus 로고    scopus 로고
    • Bridger, G. J.; Skerlj, R. T.; DeClercq, E., Ed; Jai Press: Connecticut
    • For a review on azamacrocycles as anti-HIV agents see: Advances in Antiviral Drug Design; Bridger, G. J.; Skerlj, R. T.; DeClercq, E., Ed; Jai Press: Connecticut, 1999; Vol. 3, p. 161.
    • (1999) Advances in Antiviral Drug Design , vol.3 , pp. 161
  • 9
    • 0011092723 scopus 로고    scopus 로고
    • For a recent review on regioselective functionalization of tetraazacycloalkanes see: Denat F., Brandes S., Guilard R. Synlett. 5:1999;561.
    • (1999) Synlett , vol.5 , pp. 561
    • Denat, F.1    Brandes, S.2    Guilard, R.3
  • 10
    • 0011088737 scopus 로고    scopus 로고
    • 4.
    • 3) δ 29.80, 124.77, 128.74, 131.44, 132.73, 135.32, 148.86.
  • 15
    • 0011122626 scopus 로고    scopus 로고
    • 2 (1:1:18) as eluant to give compound 2 (10.9 g, 59% yield based on the aziridine) as a yellow oil. The bis-alkylated product (1.5 g, 5%) was also isolated as a yellow oil.
    • +.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.