2006
DOI: 10.1002/chin.200620190
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An Enantioselective Total Synthesis of (+)‐Ricciocarpin A.

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“…The filtrate was concentrated under reduced pressure, and the residue so obtained was subjected to flash column chromatography (silica, 1:7 v/v ethyl acetate/40−60 petroleum ether elution). Concentration of the appropriate fractions (R f = 0.2) then gave compound 9 6 (1.29 g, 91%) as a clear, yellow oil. 1 H NMR (400 MHz, CDCl 3 , δ): 7.45 (broad s, 1H), 2.67 (t, J = 6.9 Hz, 2H), 1.92 (t, J = 6.9 Hz, 2H), 1.18 (broadened s, 6H).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…The filtrate was concentrated under reduced pressure, and the residue so obtained was subjected to flash column chromatography (silica, 1:7 v/v ethyl acetate/40−60 petroleum ether elution). Concentration of the appropriate fractions (R f = 0.2) then gave compound 9 6 (1.29 g, 91%) as a clear, yellow oil. 1 H NMR (400 MHz, CDCl 3 , δ): 7.45 (broad s, 1H), 2.67 (t, J = 6.9 Hz, 2H), 1.92 (t, J = 6.9 Hz, 2H), 1.18 (broadened s, 6H).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%