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Volumn 1, Issue 1, 1999, Pages 55-58

Preparation of TADDOL derivatives for new applications

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Indexed keywords


EID: 0002689605     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990060d     Document Type: Article
Times cited : (64)

References (37)
  • 1
    • 85034146177 scopus 로고    scopus 로고
    • Part of the projected Ph.D. Thesis
    • Part of the projected Ph.D. Thesis.
  • 2
    • 85034138879 scopus 로고    scopus 로고
    • Fulbright fellow 1995/96
    • Fulbright fellow 1995/96.
  • 3
    • 85034145993 scopus 로고    scopus 로고
    • note
    • Postdoctoral fellow 1996/97, partially financed by the Deutsche Pharmazeutische Gesellschaft.
  • 4
    • 85034124348 scopus 로고    scopus 로고
    • note
    • Postdoctoral fellow 1998/99, financed by Neste Oy Foundation (Finland).
  • 5
    • 85034129092 scopus 로고    scopus 로고
    • note
    • Laboratorium für Kristallographie, Sonneggstrasse 5, ETH Zürich, CH-8092 Zürich, Switzerland.
  • 18
    • 85034147952 scopus 로고
    • Ph.D. Dissertation, University of Basel, Switzerland
    • Rothe, P. M. Ph.D. Dissertation, University of Basel, Switzerland, 1994; Bichsel, H.-U. Diplomarbeit, ETH Zürich, 1998.
    • (1994)
    • Rothe, P.M.1
  • 19
    • 0041611377 scopus 로고    scopus 로고
    • Diplomarbeit, ETH Zürich
    • Rothe, P. M. Ph.D. Dissertation, University of Basel, Switzerland, 1994; Bichsel, H.-U. Diplomarbeit, ETH Zürich, 1998.
    • (1998)
    • Bichsel, H.-U.1
  • 23
    • 0001015289 scopus 로고
    • Appel, R. Angew. Chem. 1975, 87, 863; Angew. Chem., Int. Ed. Engl. 1975, 14, 801.
    • (1975) Angew. Chem. , vol.87 , pp. 863
    • Appel, R.1
  • 24
    • 84982373258 scopus 로고
    • Appel, R. Angew. Chem. 1975, 87, 863; Angew. Chem., Int. Ed. Engl. 1975, 14, 801.
    • (1975) Angew. Chem., Int. Ed. Engl. , vol.14 , pp. 801
  • 25
    • 85034130682 scopus 로고    scopus 로고
    • note
    • f 0.58) and the obtained product recrystallized (pentane/ether 6:1 (20 mL)) to yield 2 (3.0 g, 72%). For analytical data, see Table 2 and Supporting Information.
  • 26
    • 85034124546 scopus 로고    scopus 로고
    • note
    • f 0.10) to yield 5 (2.9 g, 63%). For analytical data, see Table 2 and Supporting Information.
  • 29
    • 85034135825 scopus 로고    scopus 로고
    • note
    • The mild conditions (in the absence of Lewis acid) for this electrophilic aromatic substitution to occur, even twice (→15), are remarkable. For analogous reactions, see refs 25-27.
  • 33
    • 85034150697 scopus 로고    scopus 로고
    • note
    • For an enumeration of the routes tested so far, see the discussion in ref 15.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.