24774-92-3Relevant academic research and scientific papers
Efficient and novel synthesis of N-Aryl-N'-ethoxycarbonylthiourea and arene-bis-ethoxycarbonylthiourea derivatives catalyzed by TMEDA
Wei, Tai-Bao,Lin, Qi,Zhang, You-Ming,Wang, Hai
, p. 2205 - 2213 (2004)
A series of N-aryl-N'-ethoxycarbonyl thioureas and arene-bis- ethoxycarbonylthiourea derivatives have been synthesized in good to excellent yields under the TMEDA catalyzed conditions at room temperature.
PYRROLO [2,3-B]PYRIDINE-3-CARBOXAMIDE COMPOSITIONS AND METHODS FOR AMELIORATING HEARING LOSS
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Paragraph 0082; 00139, (2021/08/13)
N-(3-Substituted thiazol-2(3H)-ylidene)-1H-pyrrolo[2,3-b]pyridine-3-carboxamides and N-(3-substituted oxazol-2(3H)-ylidene)-1H-pyrrolo[2,3-b]pyridine-3-carboxamides (I) and (II) are disclosed. The compounds activate Yap and inhibit Lats kinases. They are therefore useful for treating hearing loss.
TMEDA-catalyzed synthesis of N-aryl-N′-ethoxycarbonyl thiourea and arene (or polymethylene)-bis-ethoxycarbonylthiourea derivatives
Lin, Qi,Zhang, You-Ming,Gao, Li-Ming,Wei, Tai-Bao,Wang, Hai
, p. 2051 - 2057 (2007/10/03)
A novel and efficient method for synthesis ethoxycarbonyl isothiocyanate and ethoxycarbonyl thioureas catalyzed by TMEDA is reported. A series of N-aryl-N′-ethoxycarbonyl thioureas and arene (or polymethylene)-bis- ethoxycarbonyl thiourea derivatives have been synthesized in good-to-excellent yields via this method at room temperature.
Microwave promoted efficient synthesis of N-aryl-N′-ethoxycarbonyl thioureas under solvent-free and phase-transfer catalysis conditions
Lin, Qi,Zhang, You-Ming,Wei, Tai-Bao,Wang, Hai
, p. 298 - 299 (2007/10/03)
A series of N-aryl-N′-ethoxycarbonyl thioureas 3a-j were synthesised under microwave irradiation, phase transfer catalysis and solvent-free conditions.
Herstellung Kondensierter 2-Alkylthio-4-hydroxypyrimidine
Haede, Werner
, p. 1417 - 1419 (2007/10/02)
Aromatic amines and alkoxycarbonyl isothiokyanate give thioureas 7.These are alkylated to S-alkylisothioureas 8, which upon heating lose alcohol to give 2-alkylthio-4-hydroxypyrimidines.
