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Volumn 28, Issue 20, 1987, Pages 2259-2262

A general approach to nucleoside 3′- and 5′- monophosphates

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Indexed keywords


EID: 0000962508     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)96095-7     Document Type: Article
Times cited : (31)

References (27)
  • 9
    • 0001635779 scopus 로고
    • Studies of Phosphorylation. III. Selective Phosphorylation of Unprotected Nucleosides
    • 2O, overnight, and (3) TBAF (excess) in THF at 25 °C for 1.5 h gave 3 (B = Cy) in only 27% yield (HPLC analysis) together with many side-products.
    • (1969) Bulletin of the Chemical Society of Japan , vol.42 , pp. 3505
    • Yoshioka1    Kato2    Takenishi3
  • 10
    • 84918459318 scopus 로고
    • For the chemical preparation of some limited nucleoside 5′-monophopsphates, see, Asakura, Tokyo
    • (1979) Kakusan (in Japanese) , pp. 112-123
    • Ikehara1
  • 14
    • 0001529564 scopus 로고
    • For enzymatic synthesis of 5′-AMP from adenosine, see, No enzymatic 3′-O-phosphorylation methods have been reported.
    • (1951) J. Biol. Chem. , vol.193 , pp. 481
    • Kornberg1    Pricer2
  • 23
    • 0021994202 scopus 로고
    • This new phosphorochloridate, bp 76°C/0.65 mmHg, was prepared by N-chlorosuccinimide oxidation of diallyl phosphonate in benzene (25 °C, 4 h), For the preparation of the phosphonate, see
    • (1985) Can. J. Chem. , vol.63 , pp. 823
    • Kamber1    Just2
  • 25
    • 84918459316 scopus 로고    scopus 로고
    • 3 by heating the 1:2 mixture at 50 °C for 2 h.
  • 27
    • 84918459315 scopus 로고    scopus 로고
    • 2 were also employable, but the yields of products decreased to some extent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.