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stirred at r.t. for 2 h. The solvent was then removed by a rotary
evaporator. The crude product was recrystallized from methanol
to afford a yellow solid 1b (226 mg, 80% yield). [α]2D5 = +12
1
1
(c = 10 mg mL−1, CH3OH : DCM = 1 : 1); H NMR (300 MHz,
DMSO-d6) δH: 5.12 (d, J = 4.0, 1H), 6.04 (d, J = 4.0, 1H),
6.16–7.90 (m, 14H), 8.36 (br, 1H), 8.86 (s, 1H) 14.66 (br, 1H);
13C NMR (75 Hz, DMSO-d6) δC: 183.67, 168.41, 160.31,
159.89, 155.22, 145.30, 139.34, 139.24, 133.45, 128.71, 128.13,
127.71, 127.36, 115.85, 111.96, 109.32, 105.29, 74.94, 62.33;
ESI-MS: m/z 811.2567 ([M + H]+, C49H39N4O6S requires
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Acknowledgements
We are very grateful for the support of this work from the
National Natural Science Foundation of China (20832001,
20972065, 21074054, 21172106) and the National Basic
Research Program of China (2010CB923303) for their financial
support.
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4028 | Org. Biomol. Chem., 2012, 10, 4024–4028
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