Enantioselective synthesis of a benzofuranic neolignan by oxidative coupling

Tetrahedron Letters

Volumn 39, Issue 20, 1998, Pages 3291-3294

  Bolzacchini, Ezio ^a   Brunow, Gosta ^b   Meinardi, Simone ^a   Orlandi, Marco ^a   Rindone, Bruno ^a   Rummakko, Petteri ^b   Setala, Harri ^b  

^a UNIVERSITY OF MILAN   (Italy)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BENZOFURAN DERIVATIVE; FERULIC ACID; HORSERADISH PEROXIDASE; NEOLIGNAN; PHENOL DERIVATIVE;

ARTICLE; CHIRALITY; DIMERIZATION; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; OXIDATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032516356     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00473-0     Document Type: Article

References (19)

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13. 11. The HRP-catalysed phenol coupling oxidation is a well known reaction used amongst others by: Katayama, Y.; Fukuzumi, T.; Mokuzay Gakkaishi, 1978, 24(9), 664-667; Donnelly, D. M. X.; Murphy, F. G.; Polonski, J.; Prangè, T.; J. Chem. Soc. Perkin Trans 1 1987, 2719-2722; Krawczyk, A. R.; Lipowska, E.; Wrobel, J. T.; Collect. Czech. Chem. Comm. 1991, 56(5), 1147-1150.
14. 11. The HRP-catalysed phenol coupling oxidation is a well known reaction used amongst others by: Katayama, Y.; Fukuzumi, T.; Mokuzay Gakkaishi, 1978, 24(9), 664-667; Donnelly, D. M. X.; Murphy, F. G.; Polonski, J.; Prangè, T.; J. Chem. Soc. Perkin Trans 1 1987, 2719-2722; Krawczyk, A. R.; Lipowska, E.; Wrobel, J. T.; Collect. Czech. Chem. Comm. 1991, 56(5), 1147-1150.
15. th Symposium on the chemistry of Natural Products, Osaka, October 1981, p. 490.
16. D = + 14° (ethyl acetate).
17. 2O. The instrument is equipped with a Diode Array detector.
18. 15. The analysis was performed using a Chiralcel OF (4.6 i.d. × 250 mm) column eluting with an isocratic gradient 50% n-exane-50% 2-propanol. The HPLC is equipped with a Diode Array detector.
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