scholarly journals Synthesis of Substituted Hydrazines from Triprotected Precursors.

1999 ◽  
Vol 53 ◽  
pp. 1127-1133 ◽  
Author(s):  
Uno Mäeorg ◽  
Tönis Pehk ◽  
Ulf Ragnarsson
Keyword(s):  
Substituted Hydrazines

Régiosélectivité d'additions de nucléophiles sur des dialkoxycarbonyle quinoxalinotropones

1983 ◽  
Vol 61 (8) ◽  
pp. 1806-1812 ◽  
Author(s):  
Alain Turck ◽  
Roland Boutte ◽  
Guy Quéguiner
Keyword(s):  
Sodium Methoxide ◽  
Carbon Nucleophiles ◽  
Ethyl Malonate ◽  
Nitrogen Nucleophiles ◽  
Substituted Hydrazines

We have studied the regioselectivity of Michael type additions on tropones attached to quinoxalines, i.e. dialkoxycarbonyl quinoxalinotropones. We used carbon nucleophiles (ethyl malonate and malononitrile), oxygen nucleophiles (sodium methoxide), sulphur nucleophiles (methyl and benzyl mercaptans), and nitrogen nucleophiles (methyl and phenylhydrazine, aniline). We have shown that, in general, these reactions lead to 1,4-monoadditions or to bridged products arising from a bis-1,4-addition process. We have determined the structures of the complexes obtained by comparison to the work of Fohlisch etal. in the homoaromatic series. For the case of substituted hydrazines, we present some evidence on the rearrangement mechanisms proposed by these authors. [Journal translation]

Oxidations of hydrazine and substituted hydrazines by hexachloroiridate(IV) in aqueous solution: Kinetic and mechanistic analyses

2018 ◽  
Vol 256 ◽  
pp. 489-496 ◽  
Author(s):  
Chunxia Nan ◽  
Jingran Dong ◽  
Hongwu Tian ◽  
Hongmei Shi ◽  
Shigang Shen ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Solution Kinetic ◽  
Substituted Hydrazines

scholarly journals REACTION OF NITRILIMINES WITH SUBSTITUTED HYDRAZINES: SYNTHESIS OF 1,2,4,5-TETRAAZA-3-PENTENES AND FORMAZANS

2011 ◽  
Vol 19 (19) ◽  
pp. 25-33
Author(s):  
Hany M. M. DALLONI
Keyword(s):  
Molecular Structure ◽  
Spectral Data ◽  
Activated Charcoal ◽  
Lithium Hydride ◽  
Substituted Hydrazines

A series of 1,2, 4, 5-tetraaza-3-pentenes 4a-j were synthesized by the reaction of appropriate nitrilimines 2 with substituted hydrazines (H2NNHCOR, R=Ph, OMe) 3. Heating the compounds 4a-j with activated charcoal in refluxing benzene oxidized to formazans 5a-j and some formazans 5fj (R = OMe) gave s-tetrazinones 6fj in presence of lithium hydride. The microanalysis and spectral data of the synthesized compounds are in fall agreement with their molecular structure.

Sign in / Sign up

Export Citation Format

Share Document