CuCl catalyzed green and efficient one-pot synthesis of aminoindolizine frameworks via three-component reactions of aldehydes, secondary amines, and terminal alkynes in PEG
CuCl catalyzes efficient synthesis of aminoindolizine scaffolds by one-pot reactions in PEG of pyridine- or quinoline-2-carboxaldehydes with secondary amines and terminal alkynes via tandem C-H activation, coupling, and cyclization reactions. The reaction
Mishra, Sarita,Naskar, Bikramaditya,Ghosh, Rina
p. 5483 - 5487
(2013/01/13)
Synthesis of aminoindolizine and quinoline derivatives via Fe(acac)TBAOH-catalyzed sequential cross-coupling-cycloisomerization reactions
Fe(acac)TBAOH-catalyzed three-component coupling-cycloisomerization reaction of aldehydes, terminal alkynes, and amines provides a diverse range of heterocyclic compounds such as aminoindolizines and quinoline derivatives. Georg Thieme Verlag Stuttgart -
Patil, Sachin S.,Patil, Sachin V.,Bobade, Vivek D.
experimental part
p. 2379 - 2383
(2011/10/12)
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