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Volumn 38, Issue 9, 1997, Pages 1509-1510

Synthesis of 2',3'-dideoxy-3'-hydroxymethylcytidine: A novel hydroformylation route

Author keywords

[No Author keywords available]

Indexed keywords

2',3' DIDEOXY 3' HYDROXYMETHYLCYTIDINE; ANTIVIRUS AGENT; UNCLASSIFIED DRUG;

EID: 0031550894     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00142-1     Document Type: Article
Times cited : (4)

References (26)
  • 13
    • 0002207056 scopus 로고
    • Strategies and chemical approaches towards oligonucleotide therapeutics
    • Testa, B.; Fuhrer, W.; Kyburz, E.; Giger, R. (Eds.) VCH Publishers, Inc.: New York
    • 5. Moser, H. E. Strategies and Chemical Approaches Towards Oligonucleotide Therapeutics. In Perspectives in Medicinal Chemistry; Testa, B.; Fuhrer, W.; Kyburz, E.; Giger, R. (Eds.) VCH Publishers, Inc.: New York, 1993; pp 275-297.
    • (1993) Perspectives in Medicinal Chemistry , pp. 275-297
    • Moser, H.E.1
  • 19
    • 0011344577 scopus 로고    scopus 로고
    • unpublished result
    • (b) Ward, J. A. unpublished result.
    • Ward, J.A.1
  • 22
    • 0011333945 scopus 로고    scopus 로고
    • German Patent Application 1,186,455 (1961); U.S. Patent 3,239,566 (1966)
    • (c) Slaugh, L. H.; Mullineaux, R. D.; German Patent Application 1,186,455 (1961); U.S. Patent 3,239,566 (1966).
    • Slaugh, L.H.1    Mullineaux, R.D.2
  • 23
    • 0011378376 scopus 로고    scopus 로고
    • 1H NMR analyses for the hydroformylation product 4a.
    • 1H NMR analyses for the hydroformylation product 4a.
  • 24
    • 0011299668 scopus 로고    scopus 로고
    • John Wiley and Sons, Inc.: New York
    • 11. Johnson, C. R. (Ed.) Organic Syntheses, John Wiley and Sons, Inc.: New York, Vol. 57; pp 11-15.
    • Organic Syntheses , vol.57 , pp. 11-15
    • Johnson, C.R.1
  • 25
    • 0011336275 scopus 로고    scopus 로고
    • U. S. Patents 4,668,651 (1987) and 4,769,498 (1988)
    • 12. Billig, E.; Abatjoglou, A. G.; Bryant, D. R.; U. S. Patents 4,668,651 (1987) and 4,769,498 (1988).
    • Billig, E.1    Abatjoglou, A.G.2    Bryant, D.R.3
  • 26
    • 0011336276 scopus 로고    scopus 로고
    • Besides eliminating the uracil to cytocine conversion, another advantage in using 3b rather than 3a was that the cytosine moiety exhibited less predisposition toward elimination from 5b.
    • 13. Besides eliminating the uracil to cytocine conversion, another advantage in using 3b rather than 3a was that the cytosine moiety exhibited less predisposition toward elimination from 5b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.