Further Oxygenated Compounds Produced from Methyl Linoleate Monohydroperoxides at the Process of Autoxidation-Reference-Cited by-同舟云学术

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Further Oxygenated Compounds Produced from Methyl Linoleate Monohydroperoxides at the Process of Autoxidation

Published:1975-10-01 Issue:10 Volume:39 Page:2027-2033
ISSN:0002-1369
Container-title:Agricultural and Biological Chemistry
language:en
Short-container-title:Agricultural and Biological Chemistry

Author:

Terao Junji¹,Matsushita Setsuro¹

Affiliation:

1. Research Institute for Food Science, Kyoto University, Kyoto

Publisher

Oxford University Press (OUP)

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/00021369.1975.10861900

Reference22 articles.

1. M. Hamberg and B. Gotthammar, Lipids, 8, 737 (1973).

2. M. Hamberg, ibid. 10, 87 (1975).

3. R. J. Horvat, W. H. McFadden, H. Ng, A. Lee, G. Puller and T. H. Applewhite, J. Amer. Oil Chem. Soc. 46, 273 (1969).

4. R. Amano, Shokuhin Eiseigaku Zasshi, 11, 439 (1970).

5. E. N. Frankel, J. Nowakowska and C. D. Evans, J. Amer. Oil Chem. Soc. 38, 161 (1961).

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1. A versatile method to fingerprint and compare the oxidative behaviour of lipids beyond their oxidative stability;Scientific Reports;2023-05-19

2. Disclosing the chemistry of oil curing by mass spectrometry using methyl linoleate as a model binder;Microchemical Journal;2022-02

3. Crosslink mechanisms of high-solids alkyd resins in the presence of reactive diluents;Progress in Organic Coatings;2000-12

4. Oxidative crosslinking of alkyd resins studied with mass spectrometry and NMR using model compounds;Journal of Coatings Technology;1998-01

5. Aqueous Oxidation of Ethyl Linoleate, Ethyl Linolenate, and Ethyl Docosahexaenoate;Bioscience, Biotechnology, and Biochemistry;1997-01

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