13315-71-4Relevant articles and documents
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Sagitullin et al.
, (1974)
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Synthesis of α-carbolines from β-(3-indolyl) ketone 0-2,4-dinitrophenyloximes
Ono, Ayako,Narasaka, Koichi
, p. 146 - 147 (2001)
α-Carbolines are synthesized from β-(3-indolyl) ketone O-2,4-dinitrophenyloximes by the treatment with sodium hydride and sodium cyanoborohydride.
Thermal rearrangement of indolyl oxime esters to pyridoindoles
Portela-Cubillo, Fernando,Surgenor, Brian A.,Aitken, R. Alan,Walton, John C.
, p. 8124 - 8127 (2008/12/22)
(Chemical Equation Presented) Acyl oximes derived from a variety of indolylalkanones underwent a ring closure sequence during FVP to afford 9H-pyrido[2,3-b]indoles. Unlike UV light promoted reactions of oxime esters, the mechanism is almost certainly not mediated by iminyl radicals but probably involves tautomerism, elimination of acetic acid, and a final electrocyclic ring closure.
Amides and sulphonamides of benzylamines having heterocyclic substituents
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, (2008/06/13)
Amides and sulphonamides of benzylamines having heterocyclic substituents are prepared by first converting the corresponding carboxylic acids into the corresponding amines and then substituting these on the amine nitrogen in a corresponding manner. The new amides and sulphonamides of benzylamines having heterocyclic substituents can be used as active compounds in medicaments, in particular in antiatherosclerotic medicaments.