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Many-membered Carbon Rings. XI.1 Civetone Homologs

Cite this: J. Am. Chem. Soc. 1955, 77, 20, 5423–5424
Publication Date (Print):October 1, 1955
https://doi.org/10.1021/ja01625a070
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    Cited By

    This article is cited by 12 publications.

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    2. Adrien Dumas, Sophie Colombel-Rouen, Idriss Curbet, Gwénael Forcher, Fabien Tripoteau, Frédéric Caijo, Pierre Queval, Mathieu Rouen, Olivier Baslé, Marc Mauduit. Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution. Catalysis Science & Technology 2019, 9 (2) , 436-443. https://doi.org/10.1039/C8CY02115E
    3. . Blomquist Cyclic Ketone Synthesis. 2010, 437-440. https://doi.org/10.1002/9780470638859.conrr094
    4. J.‐L. Gras. Selectivity. 1993, 183-185. https://doi.org/10.1002/9780470145319.ch58
    5. L. Červený, V. Růžička. Heterogen katalysierte Hydrierungen auf dem Gebiet der Synthese von Riechstoffen. Fette, Seifen, Anstrichmittel 1983, 85 (9) , 362-370. https://doi.org/10.1002/lipi.19830850906
    6. BRAJA D. MOOKHERJEE, RICHARD A. WILSON. The Chemistry and Fragrance of Natural Musk Compounds. 1982, 433-494. https://doi.org/10.1016/B978-0-12-685850-1.50017-6
    7. PAUL RYLANDER. Hydrogenation of Ketones. 1979, 82-112. https://doi.org/10.1016/B978-0-12-605355-5.50009-4
    8. A. P. G. Kieboom, F. van Rantwijk. Hydrogenation of carbon-oxygen double bonds. 1977, 69-76. https://doi.org/10.1007/978-94-011-7589-0_12
    9. G. Ohloff. Chemie der Geruchs- und Geschmacksstoffe. , 185-251. https://doi.org/10.1007/BFb0050693
    10. G. Ohloff, J. Becker, K. H. Schulte‐Elte. Synthese von Exalton und racemischem Muscon aus Cyclododecanon Vorläufige Mitteilung. Helvetica Chimica Acta 1967, 50 (2) , 705-708. https://doi.org/10.1002/hlca.19670500231
    11. PAUL N. RYLANDER. Hydrogenation of Ketones. 1967, 258-290. https://doi.org/10.1016/B978-0-12-395532-6.50018-0
    12. H.H. Mathur, S.C. Bhattacharyya. Macrocyclic musk compounds—IX. Tetrahedron 1965, 21 (6) , 1537-1540. https://doi.org/10.1016/S0040-4020(01)98317-6

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