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Volumn 17, Issue 1-3, 1998, Pages 161-173

Synthesis of 5-arylthiouridines via electrophilic substitution of 5- bromouridines with diaryl disulfides

Author keywords

[No Author keywords available]

Indexed keywords

DISULFIDE; URIDINE DERIVATIVE;

EID: 0031933643     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328319808005167     Document Type: Article
Times cited : (6)

References (33)
  • 2
    • 2542435340 scopus 로고
    • van Tamelen, E. E. Ed.; Academic Press, New York
    • Sander, E. G. In Bioorganic Chemistry; van Tamelen, E. E. Ed.; Academic Press, New York, 1978; Vol. 2, pp. 273-297; Pal, B. C. J. Am. Chem. Soc., 1978, 100, 5170-5174; Chikuma T; Negishi, K; Hayatsu, H. Chem. Pharm. Bull, 1978, 26, 1746-1752.
    • (1978) Bioorganic Chemistry , vol.2 , pp. 273-297
    • Sander, E.G.1
  • 3
    • 0018178645 scopus 로고
    • Sander, E. G. In Bioorganic Chemistry; van Tamelen, E. E. Ed.; Academic Press, New York, 1978; Vol. 2, pp. 273-297; Pal, B. C. J. Am. Chem. Soc., 1978, 100, 5170-5174; Chikuma T; Negishi, K; Hayatsu, H. Chem. Pharm. Bull, 1978, 26, 1746-1752.
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 5170-5174
    • Pal, B.C.1
  • 4
    • 6844233467 scopus 로고
    • Sander, E. G. In Bioorganic Chemistry; van Tamelen, E. E. Ed.; Academic Press, New York, 1978; Vol. 2, pp. 273-297; Pal, B. C. J. Am. Chem. Soc., 1978, 100, 5170-5174; Chikuma T; Negishi, K; Hayatsu, H. Chem. Pharm. Bull, 1978, 26, 1746-1752.
    • (1978) Chem. Pharm. Bull , vol.26 , pp. 1746-1752
    • Chikuma, T.1    Negishi, K.2    Hayatsu, H.3
  • 13
    • 85007941327 scopus 로고
    • Inoue, H.; Ueda, T. Chem. Pharm. Bull., 1971, 19, 1743-1744. idem, ibid., 1978, 26, 2657-2663. Senda, S.; Hirota, K.; Asao, T. Tetrahedron Lett., 1973, 2647-2650. Idem, J. Org. Chem., 1975, 40, 353-356.
    • (1971) Chem. Pharm. Bull. , vol.19 , pp. 1743-1744
    • Inoue, H.1    Ueda, T.2
  • 14
    • 0018131063 scopus 로고
    • Inoue, H.; Ueda, T. Chem. Pharm. Bull., 1971, 19, 1743-1744. idem, ibid., 1978, 26, 2657-2663. Senda, S.; Hirota, K.; Asao, T. Tetrahedron Lett., 1973, 2647-2650. Idem, J. Org. Chem., 1975, 40, 353-356.
    • (1978) Chem. Pharm. Bull. , vol.26 , pp. 2657-2663
    • Inoue, H.1    Ueda, T.2
  • 15
    • 0015798008 scopus 로고
    • Inoue, H.; Ueda, T. Chem. Pharm. Bull., 1971, 19, 1743-1744. idem, ibid., 1978, 26, 2657-2663. Senda, S.; Hirota, K.; Asao, T. Tetrahedron Lett., 1973, 2647-2650. Idem, J. Org. Chem., 1975, 40, 353-356.
    • (1973) Tetrahedron Lett. , pp. 2647-2650
    • Senda, S.1    Hirota, K.2    Asao, T.3
  • 16
    • 0016590899 scopus 로고
    • Inoue, H.; Ueda, T. Chem. Pharm. Bull., 1971, 19, 1743-1744. idem, ibid., 1978, 26, 2657-2663. Senda, S.; Hirota, K.; Asao, T. Tetrahedron Lett., 1973, 2647-2650. Idem, J. Org. Chem., 1975, 40, 353-356.
    • (1975) J. Org. Chem. , vol.40 , pp. 353-356
    • Senda, S.1    Hirota, K.2    Asao, T.3
  • 27
    • 0343801201 scopus 로고
    • We preliminarily reported as a communication; Hirota, K.; Tomishi, T.; Maki, Y. Heterocycles, 1987, 26, 3089-3092.
    • (1987) Heterocycles , vol.26 , pp. 3089-3092
    • Tomishi, T.1    Maki, Y.2
  • 28
    • 85088600830 scopus 로고    scopus 로고
    • note
    • 2 On the other hand, the debrominated product was not detected by tlc analysis of the reaction mixture in the reaction of 1a with diphenyl disulfide.
  • 29
    • 6844234523 scopus 로고    scopus 로고
    • note
    • Although the reaction of 1b which possesses more free hydroxyl groups than 1a was also carried out in the presence of four equivalents of sodium hydride, the yield of 3a was not improved.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.