Regioselective Synthesis of 3-O-Alkyl Ethers of Ascorbic Acid without Protecting Groups in a Single Step-Reference-Cited by-同舟云学术

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Regioselective Synthesis of 3-O-Alkyl Ethers of Ascorbic Acid without Protecting Groups in a Single Step

Published:2000-01 Issue:3 Volume:56 Page:357-361
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Beifuss Uwe,Kunz Olaf,Voss Gundula

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference54 articles.

1. (a) Jacob, R. A.; Burri, B. J. Am. J. Clin. Nutr. 1996, 63, 985S.

2. (b) Halliwell, B.; Aruoma, O. I. DNA and Free Radicals; Ellis-Harwood: Chichester, 1993.

3. (c) Yagi, K.; Kondo, M.; Niki, E.; Yoshikawa, T. Oxygen Radicals; Excerpta Medica: Amsterdam, 1992.

4. (d) Halliwell, B. Drugs 1991, 42, 569.

5. (e) Halliwell, B.; Gutteridge, J. M. C. Free Radicals in Biology and Medicine; Oxford University Press: Oxford, 1989.

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1. A simple efficient synthesis and biological evaluation of 3-O-ethylascorbic acid;Bioscience, Biotechnology, and Biochemistry;2014-12-02

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3. ChemInform Abstract: Regioselective Synthesis of 3-O-Alkyl Ethers of Ascorbic Acid Without Protecting Groups in a Single Step.;ChemInform;2010-06-08

4. Regio- and Chemoselective One-Step 3-O-Alkylenation of Unprotected Ascorbic Acid Using ω-Iodoalkanols;Synlett;2009-01-15

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