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Volumn 63, Issue 2, 1998, Pages 347-355

Synthesis of methylene-expanded oxetanocin isonucleosides in both enantiomeric forms

Author keywords

[No Author keywords available]

Indexed keywords

OXETANOCIN A; OXETANOCIN DERIVATIVE; OXETANOCIN G;

EID: 0032559322     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971890c     Document Type: Article
Times cited : (33)

References (37)
  • 13
    • 0027169694 scopus 로고
    • (c) For an example of a structurally similar compound, the cyclopentene analogue in the L-series, with good anti-HIV activity, see: Katagiri, N.; Shiraishi, T.; Sato, H.; Toyota, A.; Kaneko, C.; Yusa, K.; Oh-hara, T.; Tsuruo, T. Biochem. Biophys. Res. Commun. 1992, 184, 154. Katagiri, N.; Shiraishi, T.; Toyota, A.; Sato, H.; Kaneko, C.; Aikawa, T. Chem. Pharm. Bull. 1993, 41, 1027.
    • (1993) Chem. Pharm. Bull. , vol.41 , pp. 1027
    • Katagiri, N.1    Shiraishi, T.2    Toyota, A.3    Sato, H.4    Kaneko, C.5    Aikawa, T.6
  • 32
    • 0000055068 scopus 로고    scopus 로고
    • We have observed this greatly reduced reactivity of alkyl halides with electron-withdrawing groups in the β- or even γ-position several times; for an example, see: Jung, M. E.; Parker, M. H. J. Org. Chem. 1997, 62, 7094. Parker, M. H. Ph.D. Thesis, UCLA, 1997.
    • (1997) J. Org. Chem. , vol.62 , pp. 7094
    • Jung, M.E.1    Parker, M.H.2
  • 33
    • 0000055068 scopus 로고    scopus 로고
    • Ph.D. Thesis, UCLA
    • We have observed this greatly reduced reactivity of alkyl halides with electron-withdrawing groups in the β- or even γ-position several times; for an example, see: Jung, M. E.; Parker, M. H. J. Org. Chem. 1997, 62, 7094. Parker, M. H. Ph.D. Thesis, UCLA, 1997.
    • (1997)
    • Parker, M.H.1
  • 35
    • 0030958236 scopus 로고    scopus 로고
    • (a) For a novel synthesis of L-ribose and 2-deoxy-L-ribose from D-ribose and L-arabinose, see: Jung, M. E.; Xu, Y. Tetrahedron Lett. 1997, 38, 4199.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4199
    • Jung, M.E.1    Xu, Y.2
  • 36
    • 15144358285 scopus 로고    scopus 로고
    • Manuscript in preparation
    • (b) We have also developed a de novo synthesis of 2-deoxy-L-ribose: Jung, M. E.; Nichols, C. J. Manuscript in preparation.
    • Jung, M.E.1    Nichols, C.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.