Direct oxidative lactonization of alkenoic acids mediated solely by NaIO4: beyond a simple oxidant

Author:

Kang Yan-Biao12345,Chen Xian-Min12345,Yao Chuan-Zhi12345,Ning Xiao-Shan12345

Affiliation:

1. Center of Advanced Nanocatalysis

2. Department of Chemistry

3. University of Science and Technology of China

4. Hefei

5. China

Abstract

Triflic acid-catalyzed direct oxidative lactonization of alkenoic acids mediated solely by NaIO4 without halogen salts is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Reference42 articles.

1. M. Hudlicky , Oxidations in Organic Chemistry, ACS Monograph Series 186, American Chemical Society, Washington, DC, 1990, p. 174

2. R. A. Johnson and K. B.Sharpless, in Catalytic Asymmetric Synthesis, ed. I. Ojima, Wiley-VCH, New York, Weinheim, 2nd edn, 2000, p. 357

3. A. H. Haines , in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, Oxford, 1st edn, 1991, vol. 7, p. 437

4. Vicinal Difunctionalization of Alkenes with Iodine(III) Reagents and Catalysts

5. Aerobic Palladium‐Catalyzed Dioxygenation of Alkenes Enabled by Catalytic Nitrite

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