Oppenauerova oxidace (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Oppenauerova oxidace" in Czech language version.

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R. V. Oppenauer. Eine Methode der Dehydrierung von Sekundären Alkoholen zu Ketonen. I. Zur Herstellung von Sterinketonen und Sexualhormonen. Recueil des Travaux Chimiques des Pays-Bas. 1937, s. 137–144. DOI 10.1002/recl.19370560206.
A. L. Wilds. Reduction with Aluminum Alkoxides (The Meerwein-Ponndorf-Verley Reduction). Organic Reactions. 1944, s. 178–223. DOI 10.1002/0471264180.or002.05.
L. Otvos; L. Gruber; J. Meisel-Agoston. The Meerwein-Ponndorf-Verley-Oppenauer. Investigation of the reaction mechanism with radiocarbon. Racemization of secondary alcohols. Acta chimica Academiae Scientiarum Hungaricae. 1965, s. 149–153. DOI 10.1002/0471264180.or002.05.
L. Mandell. The Mechanism of the Wettstein-Oppenauer Oxidation. Journal of the American Chemical Society. 1955, s. 3199–3201. DOI 10.1021/ja01594a061.
R. B. Woodward; N. L. Wendler; J. F. Brutschy. Quininone1. Journal of the American Chemical Society. 1945, s. 1425. DOI 10.1021/ja01225a001.
T. Ooi; H. Otsuka; T. Miura; H. Ichikawa; K. Maruoka. Practical Oppenauer (OPP) oxidation of alcohols with a modified aluminum catalyst. Organic Letters. 2002, s. 2669–2672. DOI 10.1021/ol020094c. PMID 12153205.
C. R. Graves; B. S. Zeng; S. T. Nguyen. Efficient and Selective Al-Catalyzed Alcohol Oxidation via Oppenauer Chemistry. Journal of the American Chemical Society. 2006, s. 12 596 – 12 597. DOI 10.1021/ja063842s.
Stéphane Caron; Robert W. Dugger; Sally Gut Ruggeri; John A. Ragan; David H. Brown Ripin. Large-Scale Oxidations in the Pharmaceutical Industry. Chemical Reviews. 2006, s. 2943–2989. DOI 10.1021/cr040679f. PMID 16836305.
L. S. Maria; Paval Kočovský; Jan-E. Bäckvall. Ruthenium-Catalyzed Oppenauer-Type Oxidation of 3β-Hydroxy Steroids. A Highly Efficient Entry into the Steroidal Hormones with 4-En-3-one Functionality. The Journal of Organic Chemistry. 1996, s. 6587–6590. DOI 10.1021/jo960361q. PMID 1166752.
L. Eignerova; A. Kasal. Intramolecular hydride shift in Oppenauer oxidation of some dihydroxy steroids. ChemPlusChem. 1976, s. 1056–1065. DOI 10.1135/cccc19761056.
N. A. Milas; F. X. Grossi; S. E. Penner; S. Kahn. The Synthesis of 1-[cyclohexen-1'-yl]-3-Methyl-1,3,5-Octatrien-7-One (C₁₅Ketone)¹. Journal of the American Chemical Society. 1948, s. 1292. DOI 10.1021/ja01183a522.
R. Reich; J. F. W. Keana. Oppenauer Oxidations Using 1-Methyl-4-Piperidone as the Hydride Acceptor. Synthetic Communications. 1972, s. 323. DOI 10.1080/00397917208061988.

nih.gov

ncbi.nlm.nih.gov

T. Ooi; H. Otsuka; T. Miura; H. Ichikawa; K. Maruoka. Practical Oppenauer (OPP) oxidation of alcohols with a modified aluminum catalyst. Organic Letters. 2002, s. 2669–2672. DOI 10.1021/ol020094c. PMID 12153205.
Stéphane Caron; Robert W. Dugger; Sally Gut Ruggeri; John A. Ragan; David H. Brown Ripin. Large-Scale Oxidations in the Pharmaceutical Industry. Chemical Reviews. 2006, s. 2943–2989. DOI 10.1021/cr040679f. PMID 16836305.
L. S. Maria; Paval Kočovský; Jan-E. Bäckvall. Ruthenium-Catalyzed Oppenauer-Type Oxidation of 3β-Hydroxy Steroids. A Highly Efficient Entry into the Steroidal Hormones with 4-En-3-one Functionality. The Journal of Organic Chemistry. 1996, s. 6587–6590. DOI 10.1021/jo960361q. PMID 1166752.