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17. Macrocyclic musk compounds. Part II. New syntheses of civetone, isocivetone, and dihydrocivetone from aleuritic acid. H. H. Mathur, S. C. Bhattacharyya , J. Chem. Soc. , 1963 , 114

Pattern generation with synthetic sensing systems in lipid bilayer membranes. Toshihide Takeuchi, Javier Montenegro, Andreas Hennig, Stefan Matile , Chem. Sci. , 2011 , 2 , 303

1240. Macrocyclic compounds. Part XI. A novel synthesis of civetone homologues. A. J. Hubert , J. Chem. Soc. , 1965 , 6679

Ti-direct, powerful, stereoselective aldol-type additions of esters and thioesters to carbonyl compounds: application to the synthesis and evaluation of lactone analogs of jasmone perfumes. Ryohei Nagase, Noriaki Matsumoto, Kohei Hosomi, Takahiro Higashi, Syunsuke Funakoshi, Tomonori Misaki, Yoo Tanabe , Org. Biomol. Chem. , 2007 , 5 , 151

Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution. Adrien Dumas, Sophie Colombel-Rouen, Idriss Curbet, Gwénael Forcher, Fabien Tripoteau, Frédéric Caijo, Pierre Queval, Mathieu Rouen, Olivier Baslé, Marc Mauduit , Catal. Sci. Technol. , 2019 , 9 , 436

A 3,4-dimercapto-3-cyclobutene-1,2-dione-chelated ruthenium carbene catalyst for Z-stereoretentive/stereoselective olefin metathesis. Tao Wang, Qingxiao Xie, Weijie Guo, Shutao Wu, Huiqing Zhang, Jianhui Wang, Botao Wu , Dalton Trans. , 2019 , 48 , 6473

Sensing applications of synthetic transport systems. Toshihide Takeuchi, Stefan Matile , Chem. Commun. , 2013 , 49 , 19

Ethenolysis of ricinoleic acid methyl ester – an efficient way to the oleochemical key substance methyl dec-9-enoate. A. Behr, S. Krema, A. Kämper , RSC Adv. , 2012 , 2 , 12775

Bicyclic analogues of exaltone (cyclopentadecanone) and muscone (3-methylcyclopentadecanone). Bruce A. McAndrew, Stephen W. Russell , J. Chem. Soc., Perkin Trans. 1 , 1975 , 1172

Notes. C.-Y. Chen, R. J. W. Le Fèvre, K. K. Chakravarti, U. G. Nayak, S. C. Bhattacharyya, V. K. Balakrishnan, R. K. Razdan, A. S. Kertes, P. J. Lloyd, J. A. Reader, P. W. G. Smith, N. Boden, J. Feeney, L. H. Sutcliffe, R. J. Ferrier, W. G. Overend, A. E. Ryan, Johannes Dale, Raymond Coulon, H. El Khadem, M. M. Abdel Rahman, G. Birch, C. W. Bird, J. H. Knox, J. M. C. Turner, M. C. Ganorkar, M. H. B. Stiddard, D. A. H. Taylor, S. Nadkarni, N. R. Williams, A. H. Jackson, A. E. Smith, J. McKechnie, D. S. Payne, W. Sim, W. J. Feast, R. Stephens , J. Chem. Soc. , 1965 , 3473