Molecules 2000, 5(10), 1094-1100; doi:10.3390/51001094
Article

Synthesis of Regioselectively Protected Protocatechuic Acid Derivatives by Biomimetic Transformation of Quinic Acid

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Received: 7 April 2000; in revised form: 11 September 2000 / Accepted: 19 September 2000 / Published: 31 October 2000
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Abstract: 3- and 4-monoesterified protocatechuic acid methyl ester (5 and 7 respectively) have been synthesised from quinic acid by a high yields biomimetic rearrangement.
Keywords: protocatechuic acid; quinic acid; diastereoselective synthesis
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MDPI and ACS Style

Bianco, A.; Bonadies, F.; Melchioni, C. Synthesis of Regioselectively Protected Protocatechuic Acid Derivatives by Biomimetic Transformation of Quinic Acid. Molecules 2000, 5, 1094-1100.

AMA Style

Bianco A, Bonadies F, Melchioni C. Synthesis of Regioselectively Protected Protocatechuic Acid Derivatives by Biomimetic Transformation of Quinic Acid. Molecules. 2000; 5(10):1094-1100.

Chicago/Turabian Style

Bianco, Armandodoriano; Bonadies, Francesco; Melchioni, Cristiana. 2000. "Synthesis of Regioselectively Protected Protocatechuic Acid Derivatives by Biomimetic Transformation of Quinic Acid." Molecules 5, no. 10: 1094-1100.

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