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Volumn , Issue 12, 2003, Pages 1889-1891

Resin Linked Dipolarophiles to Mask Nitrones

Author keywords

1,3 dipolar cycloadditions; Domino reactions; Nitrones; Protecting groups; Solid phase synthesis

Indexed keywords

ACRYLIC ACID; MALEIC ACID; NITRONE DERIVATIVE; PYRROLINE DERIVATIVE; PYRROLINE N OXIDE; RESIN; UNCLASSIFIED DRUG;

EID: 0142092191     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-41459     Document Type: Article
Times cited : (23)

References (26)
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    • For examples of solid phase 1,3-dipolar cycloadditions see: (a) Lorsbach, B. A.; Kurth, M. J. Chem. Rev. 1999, 99, 1549. (b) Sammelson, R. E.; Kurth, M. J. Chem. Rev. 2001, 101, 137; and references cited therein.
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    • Lorsbach, B.A.1    Kurth, M.J.2
  • 14
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    • and references cited therein
    • For examples of solid phase 1,3-dipolar cycloadditions see: (a) Lorsbach, B. A.; Kurth, M. J. Chem. Rev. 1999, 99, 1549. (b) Sammelson, R. E.; Kurth, M. J. Chem. Rev. 2001, 101, 137; and references cited therein.
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    • Sammelson, R.E.1    Kurth, M.J.2
  • 15
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    • note
    • 1b
  • 16
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    • note
    • 5 (213.19): C, 50.71; H, 5.20; N, 6.57. Found: C, 50.70; H, 5.34; N, 6.73.
  • 18
    • 0142038135 scopus 로고    scopus 로고
    • note
    • The excess of chiral nitrone 1 was recovered spectroscopically pure and without any loss of optical purity after a filtration through a short pad of silica gel and was as such used in other cycloadditions.
  • 19
    • 0037463770 scopus 로고    scopus 로고
    • For recent examples of Mitsunobu reactions on solid phase see: (a) Semple, G.: Andersson, B.-M.; Chhajlani, V.; Georgsson, J.; Johansson, M. J.; Rosenquist, A.; Swanson, L. Bioorg. Med. Chem. Lett. 2003, 13, 1141. (b) Dahan, A.; Portnoy, M. Macromolecules 2003, 36, 1034. (c) Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. J. Chem. Soc., Perkin Trans. 1 2002, 577. (d) Rigby, J. H. ; Kondratenko, M. A. Bioorg. Med. Chem. Lett. 2002, 12, 1829. (e) Malkinson, J. P.; Falconer, R. A. Tetrahedron Lett. 2002, 43, 9549.
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 1141
    • Semple, G.1    Andersson, B.-M.2    Chhajlani, V.3    Georgsson, J.4    Johansson, M.J.5    Rosenquist, A.6    Swanson, L.7
  • 20
    • 0037465537 scopus 로고    scopus 로고
    • For recent examples of Mitsunobu reactions on solid phase see: (a) Semple, G.: Andersson, B.-M.; Chhajlani, V.; Georgsson, J.; Johansson, M. J.; Rosenquist, A.; Swanson, L. Bioorg. Med. Chem. Lett. 2003, 13, 1141. (b) Dahan, A.; Portnoy, M. Macromolecules 2003, 36, 1034. (c) Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. J. Chem. Soc., Perkin Trans. 1 2002, 577. (d) Rigby, J. H. ; Kondratenko, M. A. Bioorg. Med. Chem. Lett. 2002, 12, 1829. (e) Malkinson, J. P.; Falconer, R. A. Tetrahedron Lett. 2002, 43, 9549.
    • (2003) Macromolecules , vol.36 , pp. 1034
    • Dahan, A.1    Portnoy, M.2
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    • 0036006409 scopus 로고    scopus 로고
    • For recent examples of Mitsunobu reactions on solid phase see: (a) Semple, G.: Andersson, B.-M.; Chhajlani, V.; Georgsson, J.; Johansson, M. J.; Rosenquist, A.; Swanson, L. Bioorg. Med. Chem. Lett. 2003, 13, 1141. (b) Dahan, A.; Portnoy, M. Macromolecules 2003, 36, 1034. (c) Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. J. Chem. Soc., Perkin Trans. 1 2002, 577. (d) Rigby, J. H. ; Kondratenko, M. A. Bioorg. Med. Chem. Lett. 2002, 12, 1829. (e) Malkinson, J. P.; Falconer, R. A. Tetrahedron Lett. 2002, 43, 9549.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , pp. 577
    • Tamamura, H.1    Hori, T.2    Otaka, A.3    Fujii, N.4
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    • 0037157756 scopus 로고    scopus 로고
    • For recent examples of Mitsunobu reactions on solid phase see: (a) Semple, G.: Andersson, B.-M.; Chhajlani, V.; Georgsson, J.; Johansson, M. J.; Rosenquist, A.; Swanson, L. Bioorg. Med. Chem. Lett. 2003, 13, 1141. (b) Dahan, A.; Portnoy, M. Macromolecules 2003, 36, 1034. (c) Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. J. Chem. Soc., Perkin Trans. 1 2002, 577. (d) Rigby, J. H. ; Kondratenko, M. A. Bioorg. Med. Chem. Lett. 2002, 12, 1829. (e) Malkinson, J. P.; Falconer, R. A. Tetrahedron Lett. 2002, 43, 9549.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 1829
    • Rigby, J.H.1    Kondratenko, M.A.2
  • 23
    • 0037164670 scopus 로고    scopus 로고
    • For recent examples of Mitsunobu reactions on solid phase see: (a) Semple, G.: Andersson, B.-M.; Chhajlani, V.; Georgsson, J.; Johansson, M. J.; Rosenquist, A.; Swanson, L. Bioorg. Med. Chem. Lett. 2003, 13, 1141. (b) Dahan, A.; Portnoy, M. Macromolecules 2003, 36, 1034. (c) Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. J. Chem. Soc., Perkin Trans. 1 2002, 577. (d) Rigby, J. H. ; Kondratenko, M. A. Bioorg. Med. Chem. Lett. 2002, 12, 1829. (e) Malkinson, J. P.; Falconer, R. A. Tetrahedron Lett. 2002, 43, 9549.
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    • Malkinson, J.P.1    Falconer, R.A.2
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    • note
    • 8).
  • 26
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    • note
    • All the solid-phase reactions were monitored by FT-IR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.