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Volumn 60, Issue 39, 2004, Pages 8669-8675

Gaining diversity in solid-phase synthesis by modulation of cleavage conditions from hydroxymethyl-based supports. Application to lamellarin synthesis

Author keywords

Acidolytic cleavage; Combinatorial chemistry; Diversity; Libraries

Indexed keywords

ALKALOID; LAMELLARIN; LEWIS ACID; UNCLASSIFIED DRUG;

EID: 4344701047     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.05.119     Document Type: Article
Times cited : (26)

References (36)
  • 4
    • 9344239161 scopus 로고    scopus 로고
    • H.-Y. Mei, & A.W. Czarnik. New York, NY: Marcel Dekker
    • Lebl M. Mei H.-Y., Czarnik A.W. Integrated Drug Discovery Technologies. 2002;395-405 Marcel Dekker, New York, NY
    • (2002) Integrated Drug Discovery Technologies , pp. 395-405
    • Lebl, M.1
  • 7
    • 0003767945 scopus 로고    scopus 로고
    • S.A. Kates, & F. Albericio. New York, USA: Marcel Dekker
    • Kates S.A., Albericio F. Solid-Phase Synthesis. A Practical Guide. 2000;Marcel Dekker, New York, USA
    • (2000) Solid-Phase Synthesis. a Practical Guide
  • 9
  • 15
    • 4344629902 scopus 로고    scopus 로고
    • The 'safety-catch' resin requires an activation before cleavage
    • The 'safety-catch' resin requires an activation before cleavage
  • 16
    • 0025246635 scopus 로고
    • For the first precedent described in the literature regarding the simultaneous synthesis of a few related compounds, which are purified before being submitted to evaluation, see
    • For the first precedent described in the literature regarding the simultaneous synthesis of a few related compounds, which are purified before being submitted to evaluation, see Tjoeng F.S., Towery D.S., Bulock J.W., Whipple D.E., Fok K.F., Williams M.H., Zupec M.E., Adams S.P. Int. J. Peptide Prot. Res. 35:1990;141-146
    • (1990) Int. J. Peptide Prot. Res. , vol.35 , pp. 141-146
    • Tjoeng, F.S.1    Towery, D.S.2    Bulock, J.W.3    Whipple, D.E.4    Fok, K.F.5    Williams, M.H.6    Zupec, M.E.7    Adams, S.P.8
  • 30
    • 0033579601 scopus 로고    scopus 로고
    • and by FT-IR, making unnecessary any further blocking step.
    • The quantitative disappearance of the hydroxyl groups in both the Merrifield-OH and the Wang resins can be followed by the Quiñoá test (Kuisle, O.; Quiñoá, E.; Riguera, R. Tetrahedron 1999, 55, 14807-14812) and by FT-IR, making unnecessary any further blocking step.
    • (1999) Tetrahedron , vol.55 , pp. 14807-14812
    • Kuisle, O.1    Quiñoá, E.2    Riguera, R.3
  • 32
    • 4344698235 scopus 로고    scopus 로고
    • We believe that such unexpected chlorination could have been achieved due to the traces of chlorine in the DCM, which under strong acid medium as the TFA and the presence of highly electron-rich aromatic rings facilitate this low yield secondary reaction. To the best of our knowledge, there are not precedents in the literature of this side-reaction
    • We believe that such unexpected chlorination could have been achieved due to the traces of chlorine in the DCM, which under strong acid medium as the TFA and the presence of highly electron-rich aromatic rings facilitate this low yield secondary reaction. To the best of our knowledge, there are not precedents in the literature of this side-reaction
  • 34
    • 0030876972 scopus 로고    scopus 로고
    • Spectroscopic data was compared with the 2-methoxy-5-iodophenol synthesized by
    • Spectroscopic data was compared with the 2-methoxy-5-iodophenol synthesized by Feldman K.S. J. Org. Chem. 62:1997;4983-4990
    • (1997) J. Org. Chem. , vol.62 , pp. 4983-4990
    • Feldman, K.S.1
  • 35
    • 4344568943 scopus 로고    scopus 로고
    • C-H couplings) and NOESY (mixing time 600 ms) correlations were performed
    • C-H couplings) and NOESY (mixing time 600 ms) correlations were performed
  • 36
    • 4344624184 scopus 로고    scopus 로고
    • Assignment may be reversed
    • Assignment may be reversed


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.