126325-43-7Relevant academic research and scientific papers
A one-pot [Bmim]OH-mediated synthesis of 3-benzamidocoumarins
Yadav, Lal Dhar S.,Singh, Santosh,Rai, Vijai K.
experimental part, p. 2208 - 2212 (2009/08/07)
The first example of an ionic liquid-promoted one-pot synthesis of 3-benzamidocoumarins from salicylaldehydes and 2-pheny-1,3-oxazolan-5-one via Knoevenagel condensation-ring transformation cascades has been reported. No by-product formation, operational
Reaction of unsaturated azlactones with sulfur nucleophiles: some observations
Mukerjee, Arya K.,Rao, Laxmi,Homami, Seyed Saied,Joseph, Kiran
, p. 1383 - 1387 (2007/10/02)
Unsaturated azlactones undergo thiolysis with toluene-α-thiol, but 2-substituted (Z)-4-o-acetoxybenzylidene-4,5-dihydrooxazol-5-ones form 3-acylaminocoumarins in the presence of triethylamine.Sodium sulfide in ethanol brings about ethanolysis of the 1,5 b
Thiol-induced Conversion of (Z)-4-o-Acetoxybenzylidene-2-phenyl-4,5-dihydrooxazol-5-ones into 3-Benzoylaminocoumarins
Mukerjee, Arya K.,Joseph, Kiran,Rao, Laxmi
, p. 2611 - 2612 (2007/10/02)
Toluene-α-thiol induces cleavage of the 1,5-bond of (Z)-4-o-acetoxybenzylidene-2-phenyl-4,5-dihydrooxazol-5-ones in triethylamine-containing ethanol to give 3-benzoylaminocoumarins.
