메뉴 건너뛰기




Volumn 38, Issue 24, 1997, Pages 4199-4202

Efficient syntheses of L-ribose and 2-deoxy L-ribose from D-ribose and L-arabinose

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBOSE; RIBOSE;

EID: 0030958236     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00870-8     Document Type: Article
Times cited : (54)

References (37)
  • 2
    • 0343348456 scopus 로고    scopus 로고
    • American Chemical Society Arthur C. Cope Scholar, 1995
    • American Chemical Society Arthur C. Cope Scholar, 1995.
  • 10
    • 0028235072 scopus 로고
    • For leading references, see: a) L-DNA: Damha, M. J.; Giannaris, P. A.; Marfey, P. Biochemistry 1994, 33, 7877. Hashimoto, Y.; Iwanami, N.; Fujimori, S.; Shudo, K. J. Am. Chem. Soc. 1993, 115, 9883. Fujimori, S.; Shudo, K.; Hashimoto, Y. J. Am. Chem. Soc. 1990, 112, 7436.
    • (1994) Biochemistry , vol.33 , pp. 7877
    • Damha, M.J.1    Giannaris, P.A.2    Marfey, P.3
  • 11
    • 0000610523 scopus 로고
    • For leading references, see: a) L-DNA: Damha, M. J.; Giannaris, P. A.; Marfey, P. Biochemistry 1994, 33, 7877. Hashimoto, Y.; Iwanami, N.; Fujimori, S.; Shudo, K. J. Am. Chem. Soc. 1993, 115, 9883. Fujimori, S.; Shudo, K.; Hashimoto, Y. J. Am. Chem. Soc. 1990, 112, 7436.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9883
    • Hashimoto, Y.1    Iwanami, N.2    Fujimori, S.3    Shudo, K.4
  • 12
    • 0025086546 scopus 로고
    • For leading references, see: a) L-DNA: Damha, M. J.; Giannaris, P. A.; Marfey, P. Biochemistry 1994, 33, 7877. Hashimoto, Y.; Iwanami, N.; Fujimori, S.; Shudo, K. J. Am. Chem. Soc. 1993, 115, 9883. Fujimori, S.; Shudo, K.; Hashimoto, Y. J. Am. Chem. Soc. 1990, 112, 7436.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 7436
    • Fujimori, S.1    Shudo, K.2    Hashimoto, Y.3
  • 18
    • 0001150442 scopus 로고
    • For the synthesis of L-nucleosides from available carbohydrates, see: a) Holy, A. Collect. Czech. Chem. Commun. 1972, 37, 4072;
    • (1972) Collect. Czech. Chem. Commun. , vol.37 , pp. 4072
    • Holy, A.1
  • 21
    • 84981749734 scopus 로고
    • a) This idea is similar to the exchange of the ends of carbohydrates in Fischer's early work on the configuration of the sugars, e.g., the synthesis of L-gulose from D-glucose. See: Fischer, E.; Piloty, O. Chem. Ber. 1891, 24, 521.
    • (1891) Chem. Ber. , vol.24 , pp. 521
    • Fischer, E.1    Piloty, O.2
  • 22
    • 84985200042 scopus 로고
    • b) For a conceptually different synthesis of 5-deoxy-L-ribose from D-ribose, see: Mori, K.; Kikuchi, H. Liebigs Ann. Chem. 1989, 1267.
    • (1989) Liebigs Ann. Chem. , pp. 1267
    • Mori, K.1    Kikuchi, H.2
  • 28
    • 84980166072 scopus 로고
    • Zinner, H. Chem. Ber. 1953, 86, 817. A rotation of -55.4 ° was reported for D-ribopyranose tetraacetate.
    • (1953) Chem. Ber. , vol.86 , pp. 817
    • Zinner, H.1
  • 29
    • 0342478898 scopus 로고    scopus 로고
    • note
    • Proton and carbon NMR of all the new synthetic compounds were consistent with the assigned structures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.