Synthesis and odour evaluation of double‐bond isomers of DAMASCENOLIDE, 4‐(4‐methylpent‐3‐en‐1‐yl)‐2(5 H )‐furanone, which has a citrus‐like odour

2020 ◽  
Vol 35 (3) ◽  
pp. 341-349 ◽  
Author(s):  
Yamato Miyazawa ◽  
Teruhisa Ohashi ◽  
Kenji Kawaguchi ◽  
Naoko Tanaka ◽  
Ryo Katsuta ◽  
...  
Keyword(s):  

2015 ◽  
Vol 407 (17) ◽  
pp. 5053-5064 ◽  
Author(s):  
Rachel L. Kozlowski ◽  
J. Larry Campbell ◽  
Todd W. Mitchell ◽  
Stephen J. Blanksby


1980 ◽  
Vol 21 (42) ◽  
pp. 4123-4126 ◽  
Author(s):  
S.Richard Baker ◽  
William B. Jamieson ◽  
Stuart W. McKay ◽  
Sarah E. Morgan ◽  
David M. Rackham ◽  
...  


Tetrahedron ◽  
1981 ◽  
Vol 37 (20) ◽  
pp. 3463-3466 ◽  
Author(s):  
K.B. Sloan ◽  
N. Bodor ◽  
J. Zupan
Keyword(s):  




1979 ◽  
Vol 17 (6) ◽  
pp. 789-800 ◽  
Author(s):  
Jean Bowler ◽  
E.D. Brown ◽  
N.S. Crossley ◽  
D.W. Heaton ◽  
T.J. Lilley ◽  
...  
Keyword(s):  


Tetrahedron ◽  
1981 ◽  
Vol 37 (20) ◽  
pp. 3467-3471 ◽  
Author(s):  
K.B. Sloan ◽  
N. Bodor ◽  
R.J. Little


1980 ◽  
Vol 58 (16) ◽  
pp. 1639-1644 ◽  
Author(s):  
Gordon L. Lange ◽  
Vincent A. Pereira ◽  
Michael Weedle

2-Cyclohexenone and three methylated cyclohexenones were thermolyzed at 400 °C for 20 hours to give conversions to products in the range 11 to 45%. When three monoterpenes containing the cyclohexenone moiety were thermolyzed under the same conditions the conversions were over 75%. The major products formed were alkylated benzenes, alkylated phenols, and double bond isomers of the starting enones. Mechanisms are proposed to account for these products.



1979 ◽  
Vol 44 (4) ◽  
pp. 641-641 ◽  
Author(s):  
Lawrence T. Scott ◽  
William R. Brunsvold


Sign in / Sign up

Export Citation Format

Share Document