Location of double bonds in polyenic long-chain carboxylic acids containing a conjugated diene unit

1988 ◽  
Vol 15 (1) ◽  
pp. 1-6 ◽  
Author(s):  
G. Janssen ◽  
A. Verhulst ◽  
G. Parmentier
2019 ◽  
Vol 23 (3) ◽  
pp. 309-319 ◽  
Author(s):  
Dariusz Pyszny ◽  
Tomasz Piotrowski ◽  
Beata Orlińska

2020 ◽  
Vol 86 ◽  
pp. 123-135 ◽  
Author(s):  
Elgun E. Hasanov ◽  
Ravan A. Rahimov ◽  
Yusif Abdullayev ◽  
Ziyafaddin H. Asadov ◽  
Gulnara A. Ahmadova ◽  
...  

1986 ◽  
Vol 41 (6) ◽  
pp. 722-730 ◽  
Author(s):  
Cornelius G. Kreiter ◽  
Eduard Michels ◽  
Jürgen Kaub

11-Isopropylidene-bicyclo[4.4.1]undeca-2,4,8-triene (IBU, 1A) and five alkyl substituted de­rivatives (1B-1F) contain a conjugated diene unit and two isolated CC-double bonds, one exocyclic and one incorporated into the bicvclus, each suited for complexation to transition metals. With [Cr(CO)3(CH3CN)3] (2) 1A-1F form [Cr(CO)3(η6-IBU)] complexes (3A−3F). in which the IBU ligands are coordinated to the chromium via the diene unit and the exocyclic CC-double bond. The corresponding [Mo(CO)3(η6-IBU)] complexes (5A−5F) are obtained from the reactions of [Mo(CO)3(diglyme)] (4) with 1A−1F. In addition, the isomeric [Mo(CO)3(η6-IBU)] complexes (6A−6D) are formed, in which the IBU ligands are bound to molybdenum via the three cyclic CC-double bonds. The complexes 3A−3F, 5A−5F and 6A−6D were studied by IR and NMR spectroscopy (1H. 13C) and characterized by C, H elemental analyses. The crystal and molecular structure of 1A was determined by X-ray structure analysis.


2020 ◽  
Vol 142 (8) ◽  
pp. 4070-4078 ◽  
Author(s):  
José Augusto Berrocal ◽  
G. Henrieke Heideman ◽  
Bas F. M. de Waal ◽  
Mihaela Enache ◽  
Remco W. A. Havenith ◽  
...  

1993 ◽  
Vol 33 (5) ◽  
pp. 1129-1131 ◽  
Author(s):  
Udom Kokpol ◽  
Warinthorn Chavasiri ◽  
Vallapa Chittawong ◽  
Marc Bruce ◽  
G.N. Cunningham ◽  
...  

2015 ◽  
Vol 2 (4) ◽  
pp. 177-190 ◽  
Author(s):  
Mutsuko Hirata-Koizumi ◽  
Sakiko Fujii ◽  
Kato Hina ◽  
Mariko Matsumoto ◽  
Mika Takahashi ◽  
...  

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