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Volumn 42, Issue 22, 2001, Pages 3721-3723

Solid-phase synthesis of functionalized tropane derivatives via 1,3-dipolar cycloaddition

Author keywords

[No Author keywords available]

Indexed keywords

3 OXIDOPYRIDINIUM BETAINE; 8 AZABICYCLO[3.2.1]OCTENONE DERIVATIVE; ACID CHLORIDE DERIVATIVE; ALKENE DERIVATIVE; BETAINE DERIVATIVE; CHLORIDE; KETONE DERIVATIVE; POTASSIUM IODIDE; REAGENT; TROPANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035963066     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)00565-2     Document Type: Article
Times cited : (8)

References (23)
  • 1
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    • For reviews on tropane alkaloids see: and references cited therein
    • For reviews on tropane alkaloids see: Fodor G.R. Nat. Prod. Rep. 11:1994;603-612. and references cited therein.
    • (1994) Nat. Prod. Rep. , vol.11 , pp. 603-612
    • Fodor, G.R.1
  • 2
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    • and references cited therein
    • O'Hagan D. Nat. Prod. Rep. 17:2000;435-446. and references cited therein.
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 435-446
    • O'Hagan, D.1
  • 3
    • 0004230722 scopus 로고
    • Ed.; Academic Press: New York
    • The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1988; Vol. 33.
    • (1988) The Alkaloids , vol.33
    • Brossi, A.1
  • 4
    • 0003744391 scopus 로고    scopus 로고
    • For recent and comprehensive reviews on solid-phase organic synthesis, see: (a) Ed.; John Wiley & Sons: New York
    • For recent and comprehensive reviews on solid-phase organic synthesis, see: (a) Solid-Phase Organic Synthesis; Burgess, K., Ed.; John Wiley & Sons: New York, 2000; (b) Ley, S. V.; Baxendale, I. R.; Bream, R. N.; Jackson, P. S.; Leach, A. G.; Longbottom, D. A.; Nesi, M.; Scott, J. S.; Storer, R. I.; Taylor, S. J. J. Chem. Soc. Perkin Trans. 1 2000, 3815-4195 and references cited therein.
    • (2000) Solid-Phase Organic Synthesis
    • Burgess, K.1
  • 10
    • 85067534917 scopus 로고    scopus 로고
    • 1H NMR analysis of this polymer revealed the presence of about 10% unreacted starting REM resin, despite the use of a large excess of betaine.
    • 1H NMR analysis of this polymer revealed the presence of about 10% unreacted starting REM resin, despite the use of a large excess of betaine.
  • 11
    • 85067533212 scopus 로고    scopus 로고
    • 1H NMR of the mixture, after flash column chromatography.
    • 1H NMR of the mixture, after flash column chromatography.
  • 12
    • 85067532597 scopus 로고    scopus 로고
    • Thesis, University of Paris 6
    • Caix-Haumesser, S. Thesis, University of Paris 6, 2000.
    • (2000)
    • Caix-Haumesser, S.1
  • 14
    • 85067533178 scopus 로고    scopus 로고
    • 10
    • 10.
  • 18
    • 85067536043 scopus 로고    scopus 로고
    • 1H NMR analysis of this resin seemed to be in agreement with structure 8, which was confirmed after cleavage.
    • 1H NMR analysis of this resin seemed to be in agreement with structure 8, which was confirmed after cleavage.
  • 19
    • 0032506569 scopus 로고    scopus 로고
    • For the cleavage using DDQ see: and references cited therein
    • For the cleavage using DDQ see: Kobayashi S., Aoki Y. Tetrahedron Lett. 39:1998;9211-9214. and references cited therein.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9211-9214
    • Kobayashi, S.1    Aoki, Y.2
  • 21
    • 85067535985 scopus 로고    scopus 로고
    • 13C NMR spectra, each of these isomers was found to be a mixture of atropoisomers.
    • 13C NMR spectra, each of these isomers was found to be a mixture of atropoisomers.
  • 22
    • 85067534930 scopus 로고    scopus 로고
    • -1).
    • -1).
  • 23
    • 85067533225 scopus 로고    scopus 로고
    • 1H NMR spectrum. As for compounds 9 and 10, this product was found to be a mixture of atropoisomers
    • 1H NMR spectrum. As for compounds 9 and 10, this product was found to be a mixture of atropoisomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.