2014
DOI: 10.5935/0103-5053.20140056
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Microwave-Assisted Synthesis ofN-Heterocycles and Their Evaluation Using an Acetylcholinesterase Immobilized Capillary Reactor

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Cited by 11 publications
(13 citation statements)
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“…41 Ketene aminals were synthesized according to literature. 21,42 Briey, 1,1bis(methylthio)-2-nitroethylene (1 mmol) and diamines (1 mmol) or primary amines (2 mmol) have been reacted in EtOH at reux for 2-4 h. The precipitate has been ltered and washed by cold ethanol (82-95% yield) (Table 3).…”
Section: Resultsmentioning
confidence: 99%
“…41 Ketene aminals were synthesized according to literature. 21,42 Briey, 1,1bis(methylthio)-2-nitroethylene (1 mmol) and diamines (1 mmol) or primary amines (2 mmol) have been reacted in EtOH at reux for 2-4 h. The precipitate has been ltered and washed by cold ethanol (82-95% yield) (Table 3).…”
Section: Resultsmentioning
confidence: 99%
“…35 Again, similar conditions were utilized for the synthesis of the cyclic and acyclic nitroketene N,S-acetals 23 and 25 by the same group (Scheme 7). 36 Dunkern et al described a slightly modied protocol for the synthesis of the nitroketene N,S-acetal derivatives 28 from 15, as depicted in Scheme 8. 37 The precursor 15 was prepared by mixing 26 with MeI in DMF at room temperature.…”
Section: General Methods For the Preparation Of Acyclic And Cyclic Nimentioning
confidence: 99%
“…While using MW irradiation, Sangi et al [31] obtained several imidazolidines, oxazolidines, and benzoxazoles. As key intermediate in these reactions, they use 1,1-bis(thiomethyl)-2-nitroethylene 33, that treated with various alkyldiamines, hydroxylalkylamines, or hydroxylarylamines was leading to the desired compounds (34,35a-e,36) in good yields and reduced reaction time (20 min).…”
Section: Five Membered Ring Azaheterocycles With One and Two Heteroatomsmentioning
confidence: 99%