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Tetrahedron Letters
Volumn 30, Issue 17, 1989, Pages 2203-2206
A cyclopropano analog of 2′,3′-dideoxycytidine: stereoselective formation of a [3,1,0] bicyclic system via homologous ferrier reaction
Author keywords

[No Author keywords available]
Indexed keywords

2',3' ALPHA METHYLENE 2',3' DIDEOXYCYTIDINE; UNCLASSIFIED DRUG;
EID: 0024574002     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)99648-5     Document Type: Article
Times cited : (64)
References (9)
  • 5
    • 84918627338 scopus 로고    scopus 로고
    • 2O, the ethoxy group of 6 was replaced by an acetoxy group along with the formation of 7. The acetoxy group was eliminated during distillation; bath temp. 105–140° at 5 mm Hg. Use of a strong acid, such as p-TsOH, leads to decomposition of 7.
  • 7
    • 84918601800 scopus 로고    scopus 로고
    • 3′,4′=0 Hz.
  • 8
    • 84918633337 scopus 로고    scopus 로고
    • 3: C 53.81; H, 5.87; N,18.82. Found: C, 53.74; H, 5.81; N, 18.84.
  • 9
    • 0009214354 scopus 로고
    • Synthetic routes to 2′,3′-cyclopropanated and 2′,3′-unsaturated nucleosides
    • A related reaction has been described, in which a [4,1,0] bicyclic system was constructed from a six-membered ring.
    • (1977) Canadian Journal of Chemistry , vol.55 , pp. 3996
    • Tam1    Fraser-Reid2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.