2004
DOI: 10.3184/0308234042037310
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Thioacetamide catalysed transformation of nitriles to 2-substituted imidazolines

Abstract: The reaction of various nitriles with ethylenediamine in presence of thioacetamide as catalyst has been studied.

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Cited by 16 publications
(12 citation statements)
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“…Compounds 1b [12] and 1c [13] were prepared according to literature methods. All the other reagents were used as commercial sources.…”
Section: Generalmentioning
confidence: 99%
“…Compounds 1b [12] and 1c [13] were prepared according to literature methods. All the other reagents were used as commercial sources.…”
Section: Generalmentioning
confidence: 99%
“…The synthesis of 2‐substituted imidazolines has become of great importance and interest, not only because they are important intermediates but also because they have been found promising applications in many pharmaceutical and synthetic areas . Due to its increasing importance, a series of methods have been developed for the synthesis of 2‐substituted imidazolines starting from nitriles , esters , carboxylic acids , and amides . However, some of these methods involve disadvantages such as harsh reaction conditions and the use of highly toxic cyanide.…”
Section: Introductionmentioning
confidence: 99%
“…A good source of C‐1 for preparation of imidazolines is nitriles. Some novel conditions have been developed for this reaction, using Lewis acids, Brönsted acids, or other small molecules as catalysts, such as HCl [13d], CuCl [13e], thioacetamide [23], sulfur [13i], ZrOCl 2 [13j], silica sulfuric acid [24], 12‐tungstophosphoric acid [25], and carbon disulfide [13k].…”
Section: Introductionmentioning
confidence: 99%