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Volumn 63, Issue 1, 2007, Pages 183-190

6′-Chloro-7- or 9-(2,3-dihydro-5H-4,1-benzoxathiepin-3-yl)-7H- or 9H-purines and their corresponding sulfones as a new family of cytotoxic drugs

Author keywords

Antitumour compounds; Benzoxathiepins; Purines; Pyrimidines

Indexed keywords

1 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 5 BROMOURACIL; 1 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 5 FLUOROURACIL; 1 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 5 TRIFLUOROMETHYLURACIL; 1 [2 (2 HYDROXYMETHYLPHENYLTHIO) 1 METHOXYETHYL]URACIL; 6' CHLORO 7 (1,1 DIOXO 2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 7H PURINE; 6' CHLORO 7 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 7H PURINE; 6' CHLORO 7 [1,1 DIOXO 2 (2 HYDROXYMETHYLPHENYLTHIO) 1 METHOXYPHENYLTHIO] 1 METHOXY 7H PURINE; 6' CHLORO 9 (1 OXO 2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 9H PURINE; 6' CHLORO 9 (1,1 DIOXO 2,3 DIHYDRO 5H BENZOXATHIEPIN 3 YL) 9H PURINE; 6' CHLORO 9 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 9H PURINE; 6' CHLORO 9 [1,1 DIOXO 2 (2 HYDROXYMETHYLPHENYLTHIO) 1 METHOXYETHYL] 9H PURINE; 6' CHLORO 9 [2 (2,3 HYDROXYMETHYLPHENYLTHIO)1 METHOXYETHYL]PURINE; 6' METHOXY 9 (2,3 DIHYDRO 5H 4,1 BENZOXATHIEPIN 3 YL) 9H PURINE; CELECOXIB; FLUOROURACIL; PURINE DERIVATIVE; ROFECOXIB; URACIL DERIVATIVE;

EID: 37849186647     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.10.023     Document Type: Article
Times cited : (25)

References (24)
  • 6
    • 37949055564 scopus 로고    scopus 로고
    • note
    • For the numbering of the compounds, the atoms of the benzoxathiepin ring are tagged with numbers without primes, while those of the pyrimidine and purine bases are numbered with primes (′).
  • 7
    • 37949000096 scopus 로고    scopus 로고
    • note
    • 3 hybridized carbon bonded to oxygen and to nitrogen are known as O,N-acetals or hemiaminals.
  • 14
    • 0037714410 scopus 로고    scopus 로고
    • Synthesis of Nucleosides
    • Paquette L.A. (Ed), Wiley, New York, NY
    • Vorbrüggen H., and Ruh-Pohlenz C. Synthesis of Nucleosides. In: Paquette L.A. (Ed). Organic Reactions Vol. 55 (2000), Wiley, New York, NY 1-630
    • (2000) Organic Reactions , vol.55 , pp. 1-630
    • Vorbrüggen, H.1    Ruh-Pohlenz, C.2
  • 15
    • 0023890847 scopus 로고
    • 4 and MeCN at room temperature, while the N-9 glycosylated products were obtained from the same purines, using TMSOTf and refluxing 1,2-dichloroethane.
    • 4 and MeCN at room temperature, while the N-9 glycosylated products were obtained from the same purines, using TMSOTf and refluxing 1,2-dichloroethane.
    • (1988) J. Org. Chem. , vol.53 , pp. 1294
    • Garner, P.1    Ramakanth, S.2
  • 20
    • 0008916154 scopus 로고
    • Macdonald J.S., Haller D.G., and Mayer R.J. (Eds), J.B. Lippincott, Philadelphia, PA
    • Schnall S., and Macdonald J.S. In: Macdonald J.S., Haller D.G., and Mayer R.J. (Eds). Manual of Oncologic Therapeutics (1995), J.B. Lippincott, Philadelphia, PA 170-184
    • (1995) Manual of Oncologic Therapeutics , pp. 170-184
    • Schnall, S.1    Macdonald, J.S.2
  • 22
    • 37949031620 scopus 로고    scopus 로고
    • Campos, J. M.; Espinosa, A.; Gallo, M. A.; Gómez-Vidal, J. A.; Núñez, M. C.; Aránega, A.; Marchal, J. A.; Rodríguez-Serrano, F. Spanish Patent Application No. P200601538, 2006.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.