On the Dienone Motif of Musks: Synthesis and Olfactory Properties of Partially and Fully Hydrogenated Dienone Musks
P Kraft, S Jordi, N Denizot…
Index: Kraft, Philip; Jordi, Samuel; Denizot, Natacha; Felker, Irene European Journal of Organic Chemistry, 2014 , vol. 2014, # 3 p. 554 - 563
Full Text: HTML
Citation Number: 4
Abstract
Abstract Minimum-energy calculations and the conformation of the (11Z)-retinylidium moiety in bovine rhodopsin called into doubt that the function of the dienone motif of a new class of musk odorants 1–6 was to stiffen and planarize the compounds. To investigate the function and importance of these double bonds, the three most potent representatives of the family of dienone musks were partially and fully hydrogenated, and the products were evaluated for ...
Related Articles:
Stereocontrolled total synthesis of the triquinane marine sesquiterpene Δ9 (12)-capnellene
[Paquette, Leo A.; Stevens, Kenneth E. Canadian Journal of Chemistry, 1984 , vol. 62, p. 2415 - 2420]
[Bergman, Rolf; Magnusson, Goeran Journal of Organic Chemistry, 1986 , vol. 51, # 2 p. 212 - 217]