메뉴 건너뛰기




Volumn 42, Issue 22, 2001, Pages 3763-3766

Approaches to 2-substituted chroman-4-ones: Synthesis of (-)-pinostrobin

Author keywords

[No Author keywords available]

Indexed keywords

4 CHROMANONE DERIVATIVE; CHROMAN DERIVATIVE; PINOSTROBIN; UNCLASSIFIED DRUG;

EID: 0035963006     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)00567-6     Document Type: Article
Times cited : (45)

References (45)
  • 7
    • 0033575406 scopus 로고    scopus 로고
    • For a recent application to the synthesis of a flavanone, see:
    • For a recent application to the synthesis of a flavanone, see: Solladié, G.; Gehrold, N.; Maignan, J. Tetrahedron: Asymmetry 1999, 10, 2739-2747.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2739-2747
    • Solladié, G.1    Gehrold, N.2    Maignan, J.3
  • 15
    • 0342412830 scopus 로고    scopus 로고
    • Starting material >99% e.e. by CHIRALCEL®OJ-R™ HPLC analysis
    • Starting material >99% e.e. by CHIRALCEL®OJ-R™ HPLC analysis.
  • 17
    • 0342412831 scopus 로고    scopus 로고
    • 13C NMR and gave satisfactory mass spectra and/or elemental analysis.
    • 13C NMR and gave satisfactory mass spectra and/or elemental analysis.
  • 20
    • 0000394945 scopus 로고
    • For a review of the mechanistic and synthetic implications of peroxydisulfate reactivity, see
    • For a review of the mechanistic and synthetic implications of peroxydisulfate reactivity, see: Minisci, F.; Citterio, A.; Giordano, C. Acc. Chem. Res. 1983, 16, 27-32.
    • (1983) Acc. Chem. Res. , vol.16 , pp. 27-32
    • Minisci, F.1    Citterio, A.2    Giordano, C.3
  • 21
    • 0342847789 scopus 로고
    • 13C NMR spectra, see:
    • 13C NMR spectra, see: Momose, T.; Ozaki, Y. Tetrahedron Lett. 1976, 3699-3702; Hanaya, K.; Kudo, H.; Gohke, K.; Imaizumi, S. Bull. Chem. Soc. Jpn. 1979, 52, 2163-2164; Senda, Y.; Ishiyama, J.; Imaizumi, S.; Hanaya, K. J. Chem. Soc., Perkin Trans. 1 1977, 217-220.
    • (1976) Tetrahedron Lett. , pp. 3699-3702
    • Momose, T.1    Ozaki, Y.2
  • 22
    • 0342847788 scopus 로고
    • 13C NMR spectra, see: Momose, T.; Ozaki, Y. Tetrahedron Lett. 1976, 3699-3702; Hanaya, K.; Kudo, H.; Gohke, K.; Imaizumi, S. Bull. Chem. Soc. Jpn. 1979, 52, 2163-2164; Senda, Y.; Ishiyama, J.; Imaizumi, S.; Hanaya, K. J. Chem. Soc., Perkin Trans. 1 1977, 217-220.
    • (1979) Bull. Chem. Soc. Jpn. , vol.52 , pp. 2163-2164
    • Hanaya, K.1    Kudo, H.2    Gohke, K.3    Imaizumi, S.4
  • 23
    • 37049091686 scopus 로고
    • 13C NMR spectra, see: Momose, T.; Ozaki, Y. Tetrahedron Lett. 1976, 3699-3702; Hanaya, K.; Kudo, H.; Gohke, K.; Imaizumi, S. Bull. Chem. Soc. Jpn. 1979, 52, 2163-2164; Senda, Y.; Ishiyama, J.; Imaizumi, S.; Hanaya, K. J. Chem. Soc., Perkin Trans. 1 1977, 217-220.
    • (1977) J. Chem. Soc., Perkin Trans. 1 , pp. 217-220
    • Senda, Y.1    Ishiyama, J.2    Imaizumi, S.3    Hanaya, K.4
  • 28
    • 0343282485 scopus 로고    scopus 로고
    • Purchased from Fluka, >99% e.e. by GC.
    • Purchased from Fluka, >99% e.e. by GC.
  • 36
    • 0343717981 scopus 로고
    • For examples, see: (a)
    • For examples, see: (a) Erdtman, H. Svensk Kem. Tidskr. 1944, 56, 95-101; (b) Lindstedt, G. Acta Chem. Scand. 1950, 4, 1042-1046; (c) Wollenweber, E. Phytochemistry 1982, 20, 1462-1464; (d) Jaipetch, T.; Reutrakul, V.; Tuntiwachwuttikul, P.; Santisuk, T. Phytochemistry 1983, 22, 625-626; (e) Haberlein, H.; Tschiersch, K.-P. Biochem. Syst. Ecol. 1998, 26, 97-103.
    • (1944) Svensk Kem. Tidskr. , vol.56 , pp. 95-101
    • Erdtman, H.1
  • 37
    • 0343282484 scopus 로고
    • (b)
    • For examples, see: (a) Erdtman, H. Svensk Kem. Tidskr. 1944, 56, 95-101; (b) Lindstedt, G. Acta Chem. Scand. 1950, 4, 1042-1046; (c) Wollenweber, E. Phytochemistry 1982, 20, 1462-1464; (d) Jaipetch, T.; Reutrakul, V.; Tuntiwachwuttikul, P.; Santisuk, T. Phytochemistry 1983, 22, 625-626; (e) Haberlein, H.; Tschiersch, K.-P. Biochem. Syst. Ecol. 1998, 26, 97-103.
    • (1950) Acta Chem. Scand. , vol.4 , pp. 1042-1046
    • Lindstedt, G.1
  • 38
    • 0342847787 scopus 로고
    • (c)
    • For examples, see: (a) Erdtman, H. Svensk Kem. Tidskr. 1944, 56, 95-101; (b) Lindstedt, G. Acta Chem. Scand. 1950, 4, 1042-1046; (c) Wollenweber, E. Phytochemistry 1982, 20, 1462-1464; (d) Jaipetch, T.; Reutrakul, V.; Tuntiwachwuttikul, P.; Santisuk, T. Phytochemistry 1983, 22, 625-626; (e) Haberlein, H.; Tschiersch, K.-P. Biochem. Syst. Ecol. 1998, 26, 97-103.
    • (1982) Phytochemistry , vol.20 , pp. 1462-1464
    • Wollenweber, E.1
  • 39
    • 0000011027 scopus 로고
    • (d)
    • For examples, see: (a) Erdtman, H. Svensk Kem. Tidskr. 1944, 56, 95-101; (b) Lindstedt, G. Acta Chem. Scand. 1950, 4, 1042-1046; (c) Wollenweber, E. Phytochemistry 1982, 20, 1462-1464; (d) Jaipetch, T.; Reutrakul, V.; Tuntiwachwuttikul, P.; Santisuk, T. Phytochemistry 1983, 22, 625-626; (e) Haberlein, H.; Tschiersch, K.-P. Biochem. Syst. Ecol. 1998, 26, 97-103.
    • (1983) Phytochemistry , vol.22 , pp. 625-626
    • Jaipetch, T.1    Reutrakul, V.2    Tuntiwachwuttikul, P.3    Santisuk, T.4
  • 40
    • 0345131726 scopus 로고    scopus 로고
    • (e)
    • For examples, see: (a) Erdtman, H. Svensk Kem. Tidskr. 1944, 56, 95-101; (b) Lindstedt, G. Acta Chem. Scand. 1950, 4, 1042-1046; (c) Wollenweber, E. Phytochemistry 1982, 20, 1462-1464; (d) Jaipetch, T.; Reutrakul, V.; Tuntiwachwuttikul, P.; Santisuk, T. Phytochemistry 1983, 22, 625-626; (e) Haberlein, H.; Tschiersch, K.-P. Biochem. Syst. Ecol. 1998, 26, 97-103.
    • (1998) Biochem. Syst. Ecol. , vol.26 , pp. 97-103
    • Haberlein, H.1    Tschiersch, K.-P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.