141208-32-4Relevant academic research and scientific papers
Synthesis of α-chloroamides in water
Harte, Andrew J.,Gunnlaugsson, Thorfinnur
, p. 6321 - 6324 (2006)
The reaction between chloroacetyl chloride and mono- or bis-aliphatic or aromatic amines in water under basic or neutral conditions gives rise to the formation of a variety of functionalized α-chloroamides. The resulting products were obtained as solids in moderate to good yields, upon precipitation and isolation by filtration.
A heteroditopic macrocycle as organocatalytic nanoreactor for pyrroloacridinone synthesis in water
Sarkar, Piyali,Sarkar, Sayan,Ghosh, Pradyut
supporting information, p. 1505 - 1514 (2019/08/07)
A heteroditopic macrocycle is reported as an efficient organocatalytic nanoreactor for the synthesis of diversely functionalized pyrroloacridinones in aqueous medium. A library of compounds was synthesized in a one-step pathway utilizing 10 mol % of the n
Cu(II) assisted self-sorting towards pseudorotaxane formation
Saha, Subrata,Ravikumar,Ghosh, Pradyut
supporting information; experimental part, p. 6272 - 6274 (2011/07/09)
A new triamino macrocycle shows Cu(II) templated self-sorting of a pseudorotaxane out of sixteen such possibilities from the mixture of nine components of a tridentate, four bidentate ligands and four transition metal ions.
A Fluorophoric-axle-based, nonfluororescent, metallo anti-[3] pseudorotaxane: Recovery of fluorescence by means of an axle substitution reaction
Saha, Subrata,Ravikumar,Ghosh, Pradyut
scheme or table, p. 13712 - 13719 (2012/02/01)
A Cu2+-templated, multinuclear, nonfluorescent, anti-[3]pseudorotaxane was synthesized on a fluorophoric axle. The Cu 2+-templated [3]pseudorotaxane was characterized by the electrospray ionization mass spectroscopy (ESI-MS), UV/Vis
