An efficient synthesis of (-)-3-deazaaristeromycin

Tetrahedron Letters

Volumn 45, Issue 49, 2004, Pages 8981-8982

  Yang, Minmin ^a   Zhou, Jian ^a   Schneller, Stewart W ^a  

^a AUBURN UNIVERSITY   (United States)

Author keywords

3 Deazapurine; Aristeromycin; Carbocyclic nucleosides; Mitsunobu reaction

Indexed keywords

3 DEAZAARISTEROMYCIN; CYCLOPENTADIENE DERIVATIVE; IMIDAZOPYRIDINE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; MITSUNOBU REACTION; REACTION ANALYSIS;

EID: 8644290745     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.10.052     Document Type: Article

References (12)

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6. O. Mitsunobu Synthesis 1981 1 28
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9. 2: C, 60.09; H, 5.67; N, 13.14. Found: C, 60.06; H, 5.60; N, 12.79
10. 3: C, 55.64; H, 5.60; N, 12.98. Found: C, 55.87; H, 5.67; N, 12.79
11. 6) 152.38, 139.97, 139.89, 138.07, 126.90, 112.57, 97.25, 84.00, 80.93, 61.81, 61.59, 45.24, 32.93, 27.42, 25.14. The proton NMR data compares favorably with that reported for (±)-7 (J.A. Secrist, R.N. Comber, R.J. Gray, R.B. Gilroy, and J.A. Montgomery J. Med. Chem. 36 1993 2102 2106)
12. 6) 148.9, 143.5, 140.1, 129.0, 126.1, 99.3, 76.1, 72.0, 62.7, 61.0, 45.4, 28.9