A group of fatty acids with ‘tetramethylene interruption’ in the double bond system

1963 ◽  
Vol 19 (10) ◽  
pp. 522-523 ◽  
Author(s):  
Joanne L. Gellerman ◽  
H. Schlenk
1930 ◽  
Vol 3 (3) ◽  
pp. 483-484
Author(s):  
Thomas Midgley ◽  
Albert L. Henne

Abstract Isoprene has been ethylated; 4-methyl-4-octene was formed exclusively. The structure of this nonene is in agreement with the usual behavior of a conjugated double bond system. This type of addition is further evidence in favor of the hypothesis which regards the polymerization of isoprene to synthetic rubber as the formation of long chains of isoprene units linked together- by ordinary valences in the 1,4-position.


1977 ◽  
Vol 32 (9) ◽  
pp. 1003-1009 ◽  
Author(s):  
Nils Wiberg ◽  
Gerhard Hübler

The chemistry of bis(trimethylsilyl)aminoisocyanide (1) is determined by three reactive centres of the system : the hydrolyzable Si–N-bond, the oxidizable carbon in the formal oxidation state two, the additionable double bond system. Reactions of the oxygen stable compound 1 with halogens X2 or sulfenyl halides RSX as oxidizing agents gives compounds of type (Me3Si)2NNCX2 or (Me3Si)2NNCX(SR). Heterocumulenes such as CO2, CS2, RNCS (R = (Me3Si)2N), SO2 add to 1, leading to heterocycles, which decompose at higher temperatures by ring cleavage. With other heterocumulenes such as PhNCO, Me3SiNSO, Me3SiNSNSiMe3 products are found, the formation of which could be explained by reaction paths including the building and cleavage of heterocycles.


1992 ◽  
Vol 47 (11) ◽  
pp. 1628-1632 ◽  
Author(s):  
Ahmed Hafez Hussein El-Ghandour ◽  
Mohamed Kamal Ahmed Ibrahim ◽  
Ibrahim Saad Abdel-Hafiz ◽  
Mohamed Hilmy Elnagdi

A novel synthesis of derivatives of the title ring system by reacting methylpyrazolo[5,1-c]-1,2,4-triazin-6-carbonitriles (9) with sulphur and subsequent treatment of the resulting thienopyrazolotriazines with acetivated double bond system is described.


1974 ◽  
Vol 29 (9-10) ◽  
pp. 677-678 ◽  
Author(s):  
Erich Ziegler ◽  
Walter Ott ◽  
Michael Riegler

The adduct from benzylidene aniline and acetic anhydride gives 1,4-diphenyl-azetidin-2-one if heated at 210°C in diphenylmethane or diphenylsilane.


1975 ◽  
Vol 30 (11-12) ◽  
pp. 946-950 ◽  
Author(s):  
Erich Ziegler ◽  
Walter Rüf

Sulfonamides react with aromatic aniles and acetic anhydride in boiling xylene yielding N-benzylidene sulfonamides, which give readily adducts with 1-phenyl-3-methyl-5-pyrazolone.


1978 ◽  
Vol 33 (9) ◽  
pp. 1016-1019 ◽  
Author(s):  
Helmut Wipfler ◽  
Erich Ziegler ◽  
Otto S. Wolfbeis

N,N′-Dimethyl-5-anilinomethylene-barbituric acids and its thio analogues react with alkyl cyanoacetates or malodinitrile in DMF in the presence of KOH to give 1,2,3,4- Tetrahydro-7 H-pyrano[2,3-d]pyrimidines, whereas N-unsubstituted anilinomethylenebarbituric acids under the same conditiones afford 1,2,3,4-tetrahydro-pyrimidine-5-propenoic acid derivatives.


1950 ◽  
Vol 71 (10) ◽  
pp. 527-530
Author(s):  
Saburo Nagakura ◽  
Hiroaki Baba

1975 ◽  
Vol 30 (11-12) ◽  
pp. 951-953 ◽  
Author(s):  
Erich Ziegler ◽  
Walter Ruf

Benzenesulfonic amide reacts with N-methylene-tert-butylamine and acetic anhydride in boiling benzene to give 5-tert-butyl-1,3-benzenesulfonyl-perhydro-1,3,5-triazine. Sulfamide, and benzylidene aniline, and acetic anhydride (1:1:1) yield N-benzylidene sulfamide, or (1:2:2) N,N′-bis-benzylidene sulfamide.


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