A Straightforward Route to Potent Phenolic Chain‐Breaking Antioxidants by Acid‐Promoted Transposition of 1,4‐Benzo[ b ]oxathiines to Dihydrobenzo[ b ]thiophenes-Reference-Cited by-同舟云学术

A Straightforward Route to Potent Phenolic Chain‐Breaking Antioxidants by Acid‐Promoted Transposition of 1,4‐Benzo[ b ]oxathiines to Dihydrobenzo[ b ]thiophenes

Published:2015-10-06 Issue:46 Volume:21 Page:16639-16645
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Viglianisi Caterina¹,Amorati Riccardo²,Di Pietro Leonardo¹,Menichetti Stefano¹

Affiliation:

1. Department of Chemistry “Ugo Schiff”, University of Florence, Via della Lastruccia 3‐13, 50019, Sesto Fiorentino, Firenze (Italy)

2. Department of Chemistry “G. Ciamician”, University of Bologna, Via S. Giacomo 11, 40126 Bologna (Italy)

Funder

Italian MIUR

University of Bologna

ISMAC-CNR Milan

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201502650

Reference59 articles.

1. Advances in Radical-Trapping Antioxidant Chemistry in the 21st Century: A Kinetics and Mechanisms Perspective

2. Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols

3. 3-Pyridinols and 5-pyrimidinols: Tailor-made for use in synergistic radical-trapping co-antioxidant systems

4. The Reactivity of Air-Stable Pyridine- and Pyrimidine-Containing Diarylamine Antioxidants

5. Maximizing the Reactivity of Phenolic and Aminic Radical-Trapping Antioxidants: Just Add Nitrogen!

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