2013
DOI: 10.4236/gsc.2013.32a002
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Green Chemistry Approach to Fast and Highly Efficient One-Pot Synthesis of Bis-Isoxazolyl-1,2,5,6-Tetrahydro Pyridine-3-Carboxylates

Abstract:

The synthesis of the bis-isoxazolyl-1,2,5,6-tetrahydro pyridine-3-carboxylates is achieved in high yield without the production of toxic waste products by using room temperature ionic liquid (RTILs) triethyl ammonium acetate (TEAA). The RTIL TEAA played the dual role of efficient green solvent as well as recyclable catalyst.

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Cited by 6 publications
(2 citation statements)
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“…Rajanarendar et al . synthesized a series of bis ‐isoxazolyl‐1,2,5,6‐tetrahydro pyridine‐3‐carboxylate starting from two equivalents of aromatic aldehydes, two equivalents of 4‐amino‐3‐methyl‐5‐styrylisoxazole and one equivalent of ethyl acetoacetate in ionic liquid triethyl ammonium acetate (TEAA) without adding any extra catalyst at room temperature (Scheme ).…”
Section: Synthesis Of 126‐triaryl‐4‐arylamino‐ Piperidine‐3‐ene‐3‐cmentioning
confidence: 99%
“…Rajanarendar et al . synthesized a series of bis ‐isoxazolyl‐1,2,5,6‐tetrahydro pyridine‐3‐carboxylate starting from two equivalents of aromatic aldehydes, two equivalents of 4‐amino‐3‐methyl‐5‐styrylisoxazole and one equivalent of ethyl acetoacetate in ionic liquid triethyl ammonium acetate (TEAA) without adding any extra catalyst at room temperature (Scheme ).…”
Section: Synthesis Of 126‐triaryl‐4‐arylamino‐ Piperidine‐3‐ene‐3‐cmentioning
confidence: 99%
“…A room temperature ionic liquid (RTILs) triethyl ammonium acetate (TEAA) was employed to develop a highly efficient methodology for the synthesis of bis-isoxazolyl-1,2,5,6tetrahydro pyridine-3-carboxylates 12 by using isoxazole amine 9, ethyl acetoacetate 10 and aldehyde 11 along with TEAA ionic liquid, in which ionic liquid play dual role of solvent and recyclable catalyst (Scheme 2). 27 High yields, reduction in reaction time, avoids the usage of hazardous organic solvents, no byproducts formation and use of room temperature ionic liquid were made this method a greener approach.…”
Section: Using Amine As Amino Sourcementioning
confidence: 99%