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Pure Appl. Chem., 2003, Vol. 75, No. 1, pp. 1-17

http://dx.doi.org/10.1351/pac200375010001

Synthetic studies on the marine natural product halichondrins

Hyeong-wook Choi, Damtew Demeke, F.-A. Kang, Y. Kishi, K. Nakajima, P. Nowak, Z.-K. Wan and C. Xie

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA

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  • Noro Jeffery C., Kalaitzis John A., Neilan Brett A.: Bioactive Natural Products from Papua New Guinea Marine Sponges. Chemistry & Biodiversity 2012, 9, 2077. <http://dx.doi.org/10.1002/cbdv.201100292>
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  • Liu Kevin K.-C., Sakya Subas M., O’Donnell Christopher J., Flick Andrew C., Ding Hong X.: Synthetic approaches to the 2010 new drugs. Bioorganic Medicinal Chemistry 2012, 20, 1155. <http://dx.doi.org/10.1016/j.bmc.2011.12.049>
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