Electrode Oxidation of Hydrazine and Related Compounds in Liquid Ammonia Electrolytes

1970 ◽  
Vol 117 (1) ◽  
pp. 60 ◽  
Author(s):  
M. H. Miles ◽  
P. M. Kellett
1956 ◽  
Vol 9 (3) ◽  
pp. 391 ◽  
Author(s):  
J Cymerman-Craig ◽  
M Moyle ◽  
P Rowe-Smith ◽  
PC Wailes

Attempted condensation of benzil and benzoin with sodium acetylide in liquid ammonia caused fission of the central carbon-carbon bond of these substances, giving 3-phenylprop-1-yn-3-ol. Condensation of α-bromodeoxyanisoin with the same reagent gave several non-acetylenic products which have been identified.


1963 ◽  
Vol 11 (12) ◽  
pp. 1477-1483 ◽  
Author(s):  
Masao Tomita ◽  
Tohru Kikuchi ◽  
Kiyoshi Bessho ◽  
Yasuo Inubushi

1988 ◽  
Vol 61 (5) ◽  
pp. 1647-1651 ◽  
Author(s):  
Ryu Sato ◽  
Satoru Saito ◽  
Hiroshi Chiba ◽  
Takehiko Goto ◽  
Minoru Saito

1981 ◽  
Vol 46 (12) ◽  
pp. 3134-3144 ◽  
Author(s):  
Antonín Holý

Reaction of 9-((RS)-2,3-dihydroxypropyl)adenine (I) with p-toluenesulfonyl chloride afforded the 3-O-p-toluenesulfonyl derivative II which on treatment with 2,3-dihydropyran was transformed into the 3-O-p-toluenesulfonyl-2-O-tetrahydropyranyl derivative III. Reaction of II with sodium isobutyl mercaptide in liquid ammonia gave 9-((RS)-3-isobutylthio-2-hydroxypropyl)adenine (IV). Analogously, compound III and disodium salt of L-homocysteine after acid hydrolysis afforded S-((RS)-3-(adenin-9-yl)-2-hydroxypropyl)-L-homocysteine (V). 9-((2S,3S)-threo-2,3-O-Isopropylidene-4-O-p-toluenesulfonyl-2,3,4-trihydroxybutyl)adenine (VIII) was transformed in a similar way into the 4-isobutylthio derivative IX and the L-homocysteine derivative X. 9-Allyladenine (XII) on treatment with bromine in dioxane afforded 9-((RS)-2,3-dibromopropyl)adenine (XIII) and probably 3,9-(2-bromotrimethylene)adeninium bromide (XIV). Reaction of compounds XIII, XIV and 9-((RS)-2,3-bis-p-toluenesulfonyloxypropyl)adenine (XI) with sodium hydrogen sulfide or sodium thioacetate led invariably to polymeric compounds. 4-p-Toluenesulfonyloxymethyl-2,2-dimethyl-1,3-dithiolane (XVa) reacted with sodium salt of adenine to give 9-(X)-2,2-dimethyl-1,3-dithiolane-4-ylmethyl)adenine (XVIa); analogously, 4-p-toluenesulfonyloxymethyl-2-phenyl-1,3-dithiolane (XVb) afforded the 2,3-S-benzylidene derivative XVIb and 1-p-toluenesulfonyloxy-2,3-bis(benzylthio)propane (XIXb) gave 9-((RS)-2,3-bis(benzylthio)propyl)adenine (XIXc). Acetolysis of XVIa or reduction of XVIb with sodium in liquid ammonia led to 9-((RS)-2,3-dimercaptopropyl)adenine (XVIII) and the corresponding episulfide XVII.


1992 ◽  
Vol 47 (11) ◽  
pp. 1571-1579 ◽  
Author(s):  
Falk Olbrich ◽  
Bärbel Zimmer ◽  
Michael Kastner ◽  
Carl von Schlabrendorff ◽  
Gottlieb Vetter ◽  
...  

X-ray analysis shows silver(I) aminomethylnitrosolate to have dimers as structural units, in which the W-shaped nitrosolate ions act as μ2-bridging ligands via the nitrogen atoms of the NO groups. The nearly planar dinuclear complexes form stacks, which are connected by additional AgO contacts leading to a kind of layer structure. These layers are held together by hydrogen bonds.Mononuclear complexes of composition [Ag(nitrosolate)L2] can be obtained from silver(I) ethylnitrosolate and bipyridyl in methanol and from silver(I) benzylnitrosolate and triphenylphosphane in diethylether/liquid ammonia. In these complexes the nitrosolate ions are supposed to act as chelating ligands, again with N,N′-coordination.


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