The Synthesis and Regioselective Hydrolysis of Dialkyl 2-Phenylfuran (and 2-Phenyltetrahydrofuran)-3,4-dicarboxylates

Shrong Shi LIN Bo YANG

引用本文: Shrong Shi LIN,  Bo YANG. The Synthesis and Regioselective Hydrolysis of Dialkyl 2-Phenylfuran (and 2-Phenyltetrahydrofuran)-3,4-dicarboxylates[J]. Chinese Chemical Letters, 2002, 13(9): 826-829. shu
Citation:  Shrong Shi LIN,  Bo YANG. The Synthesis and Regioselective Hydrolysis of Dialkyl 2-Phenylfuran (and 2-Phenyltetrahydrofuran)-3,4-dicarboxylates[J]. Chinese Chemical Letters, 2002, 13(9): 826-829. shu

The Synthesis and Regioselective Hydrolysis of Dialkyl 2-Phenylfuran (and 2-Phenyltetrahydrofuran)-3,4-dicarboxylates

摘要: Dialkyl 2-phenylfuran (and 2-phenyltetrahydrofuran)-3,4-dicarboxylates (1, 2, 5-7), which are potential precursors of the synthesis of furofuran and tetrahydrofurofuran lignans, can be selectively hydrolyzed to monoacid (3, 8) by potassium hydroxide. The regioselective hydrolysis was affected significantly by the 2-phenyl group of the furan or tetrahydrofuran skeleton. The geometric structures of 3, 8 and related compounds were elucidated and verified by NMR spectra.

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  • 收稿日期:  2002-01-25
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