메뉴 건너뛰기




Volumn 47, Issue 26, 2004, Pages 6476-6484

Calcitriol derivatives with two different side chains at C-20. II. Diastereoselective syntheses of the metabolically produced 24(R)-hydroxygemini

Author keywords

[No Author keywords available]

Indexed keywords

19 NORCALCITRIOL; CALCITRIOL DERIVATIVE; GAMMA INTERFERON; UNCLASSIFIED DRUG;

EID: 10644257331     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm049340b     Document Type: Article
Times cited : (12)

References (22)
  • 1
    • 10644243769 scopus 로고    scopus 로고
    • July 6-10, 2003, Maastricht, The Netherlands, Abstracts, Reference 18
    • This paper was presented in part at the 12th Workshop on Vitamin D, July 6-10, 2003, Maastricht, The Netherlands, Abstracts, p 41. Part I: Reference 18.
    • 12th Workshop on Vitamin D , Issue.1 PART , pp. 41
  • 3
    • 10644242054 scopus 로고    scopus 로고
    • 3 analogs with bis-C-20 side chains for treating or preventing neoplastic diseases, US 6008209, 1999, 13 pp.
    • 3 analogs with bis-C-20 side chains for treating or preventing neoplastic diseases, US 6008209, 1999, 13 pp.
    • Manchand, P.S.1    Uskokovic, M.R.2
  • 4
    • 10644244619 scopus 로고    scopus 로고
    • 3 analogs with bis-C-20 side chains as therapeutic agents, WO 9849138 1998, 35 pp.
    • 3 analogs with bis-C-20 side chains as therapeutic agents, WO 9849138 1998, 35 pp.
    • Manchand, P.S.1    Uskokovic, M.R.2
  • 6
    • 0034835474 scopus 로고    scopus 로고
    • Double bond in the side chain of 1α,25-dihydroxy-22-ene-vitamin D3 is reduced during its metabolism: Studies in chronic myeloid leukemia (RWLeu-4) cells and rat kidney
    • Rao, S.; Balkundi, D.; Uskokovic, M. R.; Tserng, K.-Y.; Clark, J. W.; Horst, R. L.; Reddy, G. S. Double bond in the side chain of 1α,25- dihydroxy-22-ene-vitamin D3 is reduced during its metabolism: Studies in chronic myeloid leukemia (RWLeu-4) cells and rat kidney. J. Steroid Biochem. Mol. Biol. 2001, 78, 167-176.
    • (2001) J. Steroid Biochem. Mol. Biol. , vol.78 , pp. 167-176
    • Rao, S.1    Balkundi, D.2    Uskokovic, M.R.3    Tserng, K.-Y.4    Clark, J.W.5    Horst, R.L.6    Reddy, G.S.7
  • 14
    • 10644234976 scopus 로고    scopus 로고
    • Preparation of intermediates for the synthesis of 19-nor-vitamin D compounds. US 5086191, 1992
    • (b) DeLuca, H. F.; Schnoes, H. K.; Perlman, K. L. Preparation of intermediates for the synthesis of 19-nor-vitamin D compounds. US 5086191, 1992.
    • DeLuca, H.F.1    Schnoes, H.K.2    Perlman, K.L.3
  • 15
    • 10644281557 scopus 로고    scopus 로고
    • Novel synthesis of 19-nor-vitamin D compounds. EP 516410, 1992
    • (c) Deluca, H. F.; Schnoes, H. K.; Perlman, K. L.; Swenson, R. E. Novel synthesis of 19-nor-vitamin D compounds. EP 516410, 1992.
    • Deluca, H.F.1    Schnoes, H.K.2    Perlman, K.L.3    Swenson, R.E.4
  • 16
    • 0036662355 scopus 로고    scopus 로고
    • Graphic representation of configuration in two-dimensional space. Current conventions, clarifications, and proposed extensions
    • Chemical structures are drawn according to a proposed convention: Maehr, H. Graphic representation of configuration in two-dimensional space. Current conventions, clarifications, and proposed extensions. J. Chem. Inf. Comput. Sci. 2002, 42, 894-902.
    • (2002) J. Chem. Inf. Comput. Sci. , vol.42 , pp. 894-902
    • Maehr, H.1
  • 17
    • 0000224988 scopus 로고
    • Synthetic approaches to vitamin D and its relatives
    • Lythgoe, B. Synthetic approaches to vitamin D and its relatives. Chem. Soc. Rev. 1981, 10, 449-475.
    • (1981) Chem. Soc. Rev. , vol.10 , pp. 449-475
    • Lythgoe, B.1
  • 18
    • 11944270778 scopus 로고
    • Synthesis of vitamin D (calciferol)
    • Zhu, G.-D.; Okamura, W. H. Synthesis of vitamin D (calciferol). Chem. Rev. 1995, 95, 1877-1952.
    • (1995) Chem. Rev. , vol.95 , pp. 1877-1952
    • Zhu, G.-D.1    Okamura, W.H.2
  • 19
    • 0022442161 scopus 로고
    • Stereocontrolled total synthesis of 1α,25-dihydroxycholecalciferol and 1α,25-dihydroxyergocalciferol
    • Baggiolini, E. G.; Iacobelli, J. A.; Hennessy, B. M.; Batcho, A. D.; Sereno, J. F.; Uskokovic, M. R. Stereocontrolled total synthesis of 1α,25-dihydroxycholecalciferol and 1α,25-dihydroxyergocalciferol. J. Org. Chem. 1986, 51, 3098-3108.
    • (1986) J. Org. Chem. , vol.51 , pp. 3098-3108
    • Baggiolini, E.G.1    Iacobelli, J.A.2    Hennessy, B.M.3    Batcho, A.D.4    Sereno, J.F.5    Uskokovic, M.R.6
  • 21
    • 3042651921 scopus 로고    scopus 로고
    • Formal desymmetrization of the diastereomeric chains in gemini calcitriol derivatives with two different side chains at C-20
    • Maehr, H.; Uskokovic, M. R. Formal desymmetrization of the diastereomeric chains in gemini calcitriol derivatives with two different side chains at C-20. Eur. J. Org. Chem. 2004, 1703-1713.
    • (2004) Eur. J. Org. Chem. , pp. 1703-1713
    • Maehr, H.1    Uskokovic, M.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.