Oppenauer oxidation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Oppenauer oxidation" in English language version.

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12doi.org

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4nih.gov

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doi.org

Oppenauer, R. V. (1937). "Eine Methode der Dehydrierung von Sekundären Alkoholen zu Ketonen. I. Zur Herstellung von Sterinketonen und Sexualhormonen" [Dehydration of secondary alcohols to ketones. I. Preparation of sterol ketones and sex hormones]. Recl. Trav. Chim. Pays-Bas (in German). 56 (2): 137–144. doi:10.1002/recl.19370560206.
Wilds, A. L. (1944). "Reduction with Aluminum Alkoxides (The Meerwein-Ponndorf-Verley Reduction)". Org. React. 2 (5): 178–223. doi:10.1002/0471264180.or002.05.
Mandell, L. (1955). "The Mechanism of the Wettstein-Oppenauer Oxidation". J. Am. Chem. Soc. 78 (13): 3199–3201. doi:10.1021/ja01594a061.
Woodward, R. B.; Wendler, N. L.; Brutschy, F. J. (1945). "Quininone1". J. Am. Chem. Soc. 67 (9): 1425. doi:10.1021/ja01225a001.
Ooi, T.; Otsuka, H.; Miura, T.; Ichikawa, H.; Maruoka, K. (2002). "Practical Oppenauer (OPP) oxidation of alcohols with a modified aluminum catalyst". Organic Letters. 4 (16): 2669–72. doi:10.1021/ol020094c. PMID 12153205.
Graves, C. R.; Zeng, B. S.; Nguyen, S. T. (2006). "Efficient and Selective Al-Catalyzed Alcohol Oxidation via Oppenauer Chemistry". Journal of the American Chemical Society. 128 (39): 12596–7. doi:10.1021/ja063842s. PMID 17002323.
Stéphane Caron; Robert W. Dugger; Sally Gut Ruggeri; John A. Ragan & David H. Brown Ripin (2006). "Large-Scale Oxidations in the Pharmaceutical Industry". Chem. Rev. 106 (7): 2943–89. doi:10.1021/cr040679f. PMID 16836305.
Almeida, Maria L.S.; Kočovský, Paval; Bäckvall, Jan-E. (1996). "Ruthenium-Catalyzed Oppenauer-Type Oxidation of 3β-Hydroxy Steroids. A Highly Efficient Entry into the Steroidal Hormones with 4-En-3-one Functionality". J. Org. Chem. 61 (19): 6587–6590. doi:10.1021/jo960361q. PMID 11667525.
Eignerova, L.; Kasal, A. (1976). "Intramolecular hydride shift in Oppenauer oxidation of some dihydroxy steroids". ChemPlusChem. 41 (4): 1056–1065. doi:10.1135/cccc19761056.
Milas, N. A.; Grossi, F. X.; Penner, S. E.; Kahn, S. (1948). "The Synthesis of 1-[cyclohexen-1'-yl]-3-Methyl-1,3,5-Octatrien-7-One (C₁₅Ketone)¹". Journal of the American Chemical Society. 70 (3): 1292. doi:10.1021/ja01183a522.
Reich, R.; Keana, J. F. W. (1972). "Oppenauer Oxidations Using 1-Methyl-4-Piperidone as the Hydride Acceptor". Synthetic Communications. 2 (5): 323. doi:10.1080/00397917208061988.
Reich, Richard; Keana, John F. W. (1972). "Oppenauer Oxidations Using 1-Methyl-4-Piperidone as the Hydride Acceptor". Synthetic Communications. 2 (5): 323–325. doi:10.1080/00397917208061988.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ooi, T.; Otsuka, H.; Miura, T.; Ichikawa, H.; Maruoka, K. (2002). "Practical Oppenauer (OPP) oxidation of alcohols with a modified aluminum catalyst". Organic Letters. 4 (16): 2669–72. doi:10.1021/ol020094c. PMID 12153205.
Graves, C. R.; Zeng, B. S.; Nguyen, S. T. (2006). "Efficient and Selective Al-Catalyzed Alcohol Oxidation via Oppenauer Chemistry". Journal of the American Chemical Society. 128 (39): 12596–7. doi:10.1021/ja063842s. PMID 17002323.
Stéphane Caron; Robert W. Dugger; Sally Gut Ruggeri; John A. Ragan & David H. Brown Ripin (2006). "Large-Scale Oxidations in the Pharmaceutical Industry". Chem. Rev. 106 (7): 2943–89. doi:10.1021/cr040679f. PMID 16836305.
Almeida, Maria L.S.; Kočovský, Paval; Bäckvall, Jan-E. (1996). "Ruthenium-Catalyzed Oppenauer-Type Oxidation of 3β-Hydroxy Steroids. A Highly Efficient Entry into the Steroidal Hormones with 4-En-3-one Functionality". J. Org. Chem. 61 (19): 6587–6590. doi:10.1021/jo960361q. PMID 11667525.