Synthesis of 6-substituted 5-cyano-7-hydroxy-2-carboxybenzofurans
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References and notes (9)
- et al.
Pharmacol. Ther.
(2009) - et al.
Expert Opin. Ther. Patents
(2008) - et al.
J. Org. Chem.
(2002)et al.J. Org. Chem.
(2006)
There are more references available in the full text version of this article.
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