1268673-01-3Relevant academic research and scientific papers
Synthesis of pyrido[2,3-b]indoles and pyrimidoindoles via Pd-catalyzed amidation and cyclization
Kumar, Arepalli Sateesh,Amulya Rao,Nagarajan, Rajagopal
supporting information; experimental part, p. 5084 - 5093 (2012/08/07)
Biologically and pharmaceutically active core structures containing a new class of 4-hydroxy-α-carbolines, dihydropyrido[2,3-b]indoles, pyrimido[4,5-b] and [5,4-b]indoles have been synthesized in good yields via Pd-catalyzed amidation and cyclizations. The keto-enol tautomerism in 4-hydroxy-α-carbolines has been investigated by DFT calculations and spectroscopic techniques. The fluorescence studies of pyrimido[4,5-b] and [5,4-b]indoles were carried out with good quantum yields.
Synthesis of α-carbolines via Pd-catalyzed amidation and Vilsmeier-Haack reaction of 3-acetyl-2-chloroindoles
Kumar, Arepalli Sateesh,Nagarajan, Rajagopal
supporting information; experimental part, p. 1398 - 1401 (2011/05/03)
A new class of α-carboline derivatives has been synthesized by Pd2(dba)3/BINAP catalyzed amidation of 3-acetyl-2-chloroindoles followed by a Vilsmeier-Haack reaction and is reported.
