147848-01-9Relevant academic research and scientific papers
Synthesis of di-, tri-, and tetra-substituted carbazole analogs involving annulation methodology
Ramesh, Neelamegam,Rajeshwaran, Ganesan Gobi,Mohanakrishnan, Arasambattu K.
experimental part, p. 3592 - 3602 (2009/09/06)
Synthesis of substituted carbazole analogs was achieved via Michael addition followed by intramolecular cyclization and subsequent aromatization.
Facile preparation of indolyl-2/3-methylsulfoxides using HF/H 2O2
Rajeshwaran, Ganesan Gobi,Ramesh, Neelamegam,Mohanakrishnan, Arasambattu K.
experimental part, p. 1215 - 1227 (2009/10/09)
A variety of indolyl-2/3-methylsulfides tethered with sensitive functionalities were oxidized to the corresponding sulfoxides using a hitherto unexplored HF/H2O2 system. Copyright Taylor & Francis Group, LLC.
An efficient preparation of 1-phenylsulfonylindolyl methyl sulfoxides using KF/m-CPBA
Mohanakrishnan, Arasambattu K.,Ramesh, Neelamegam
, p. 4231 - 4233 (2007/10/03)
A variety of 1-phenylsulfonylindolylmethyl sulfides are selectively oxidized to the corresponding sulfoxides using a hitherto unexplored KF/m-CPBA system. A major advantage is the absence of over-oxidation.
One pot synthesis of 4-hydroxy-3-substituted carbazoles via sulfoxide stabilised carbanion
Mohanakrishnan,Srinivasan
, p. 1343 - 1346 (2007/10/02)
A convenient method for the synthesis of 4-hydroxy-3-substituted carbazoles (Potential intermediate for pyridocarbazole alkaloids) from ethyl 5-methoxy-2-phenylsulfinylmethyl-1-phenylsulfonylindole-3-carboxylate is reported.
