2011
DOI: 10.1080/00397911.2010.494818
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Novel and Efficient One-Pot Synthesis of (Aminophenyl)carbamic Acid Esters

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Cited by 4 publications
(5 citation statements)
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“…Finally, the signals between 6.95 and 7.55 ppm were assigned to the aryl protons of toluene dicarbamate isomers (TDC); the even higher chemical shifts are due to the presence of two carbamate groups. These trends of the chemical shifts in the mono‐ and dicarbamates were confirmed by comparison with the spectra of the corresponding mono‐ and diethylcarbamates …”
Section: Resultsmentioning
confidence: 88%
“…Finally, the signals between 6.95 and 7.55 ppm were assigned to the aryl protons of toluene dicarbamate isomers (TDC); the even higher chemical shifts are due to the presence of two carbamate groups. These trends of the chemical shifts in the mono‐ and dicarbamates were confirmed by comparison with the spectra of the corresponding mono‐ and diethylcarbamates …”
Section: Resultsmentioning
confidence: 88%
“…Kayu jati juga memiliki banyak senyawa bioaktif (Neamatallah et al 2005;Thulasidas et al 2006;Lacret et al 2011;Syofuna et al 2012), dan senyawa yang mampu menghilangkan logam berat (Rao et al 2010). Beberapa senyawa telah diisolasi dari hampir setiap bagian jati seperti senyawa steroid, asam fenolat, dan senyawa antioksidan (Lukmandaru & Takahashi 2008;Gorafalo et al 2011;Setiawan et al 2013).…”
Section: Pendahuluanunclassified
“…40−42 The synthesis of (aminophenyl)carbamic acid esters 11−27 was performed by a one-pot reduction procedure of the corresponding nitrophenyl isocyanate in the presence of various alcohols in a CH 2 Cl 2 /THF mixture. 46 Condensation of 1,4phenylenediamine and the corresponding isocyanate in CHCl 3 afforded the desired ureas 28−32 in high yields and short reaction times. 47 Amide analogues 33 and 34 were prepared from 2methyl-4-nitroaniline according to a two-step procedure: acetylation from chloride derivatives and reduction under a hydrogen atmosphere using Raney nickel as the catalyst.…”
Section: ■ Chemistrymentioning
confidence: 99%
“…The synthesis of (aminophenyl)­carbamic acid esters 11 – 27 was performed by a one-pot reduction procedure of the corresponding nitrophenyl isocyanate in the presence of various alcohols in a CH 2 Cl 2 /THF mixture . Condensation of 1,4-phenylenediamine and the corresponding isocyanate in CHCl 3 afforded the desired ureas 28 – 32 in high yields and short reaction times .…”
Section: Chemistrymentioning
confidence: 99%
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