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Volumn 7, Issue 11, 1999, Pages 2373-2379

Synthesis and anti-HIV evaluation of 2',3'-dideoxy imidazo- and ν- triazolo[4,5-d]pyridazine nucleosides

Author keywords

triazolopyridazines; ddI analogues; Deoxynucleosides; HIV; Imidazopyridazines

Indexed keywords

1 (2,3 DIDEOXY BETA DEXTRO GLYCEROPENTOFURANOSYL)IMIDAZO[4,5 D]PYRIDAZIN 4(5H) ONE; 1 (2,3 DIDEOXY BETA DEXTRO GLYCEROPENTOFURANOSYL)TRIAZOLO[4,5 D]PYRIDAZIN 4(5H) ONE; DIDANOSINE; IMIDAZOPYRIDAZINE DERIVATIVE; NUCLEOSIDE DERIVATIVE; TRIAZOLOPYRIDAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033490797     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00184-4     Document Type: Article
Times cited : (30)

References (24)
  • 14
    • 0342884921 scopus 로고    scopus 로고
    • On larger scale reactions (e.g. 5-10 g of 3) the average yield of 4/5 was 80%
    • On larger scale reactions (e.g. 5-10 g of 3) the average yield of 4/5 was 80%.
  • 15
    • 4243620067 scopus 로고
    • + neutralization of the reaction solution led to a small amount of the α-anomer. Although efforts to prevent anomerization were made, the occurrence of the α-anomer was always detected. Personal communication from Dr. Jean-Luc Girardet. For the mechanism of anomerization see
    • + neutralization of the reaction solution led to a small amount of the α-anomer. Although efforts to prevent anomerization were made, the occurrence of the α-anomer was always detected. Personal communication from Dr. Jean-Luc Girardet. For the mechanism of anomerization see, Capon B. Chem. Rev. 1969, 69, 407.
    • (1969) Chem. Rev. , vol.69 , pp. 407
    • Capon, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.