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

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

Dipartimento di Chimica, Università “La Sapienza”, Piazzale Aldo Moro n. 5, I-00185, Roma, Italy
* Author to whom correspondence should be addressed.
Received: 7 April 2000; in revised form: 11 September 2000 / Accepted: 19 September 2000 / Published: 31 October 2000
PDF Full-text Download PDF Full-Text [74 KB, uploaded 9 October 2008 11:30 CEST]
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

Article Statistics

Load and display the download statistics.

Citations to this Article

Cite This Article

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.

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert