1025997-20-9Relevant academic research and scientific papers
A General Carbazole Synthesis via Stitching of Indole-Ynones with Nitromethanes: Application to Total Synthesis of Carbazomycin A, Calothrixin B, and Staurosporinone
Singh, Shweta,Samineni, Ramesh,Pabbaraja, Srihari,Mehta, Goverdhan
supporting information, p. 3372 - 3376 (2019/05/10)
A new, one-pot domino benzannulation reaction between indole-3-ynones and various nitromethane derivatives has been explored for a general entry to diversely functionalized carbazole frameworks (28 examples). The scope of this new benzannulation has been
New three-component glyoxylation-decarbonylative stille coupling sequence to Acyl heterocycles under mild conditions
Tasch, Boris O. A.,Merkul, Eugen,Frank, Walter,Mueller, Thomas J.J.
experimental part, p. 2139 - 2146 (2010/09/04)
A consecutive sequence of glyoxylation of 1-methyl-1H-indole, 1-(4-methoxybenzyl)-1H-pyrrolo[2,3-b]pyridine or N-substituted pyrroles with oxalyl chloride and subsequent decarbonylative Stille coupling under very mild, Lewis acid free conditions using all reactants in equimolar quantities is reported. As an illustration, this glyoxylation-decarbonylative coupling sequence was elaborated into a consecutive, four-component synthesis of 1-methyl-3-(1-methyl-4,5-dihydro-1H-pyrazol-3-yl)-1H-indole. Georg Thieme Verlag Stuttgart - New York.
Synthesis of isoxazoles via electrophilic cyclization
Waldo, Jesse P.,Larock, Richard C.
, p. 5203 - 5205 (2007/10/03)
(Chemical Equation Presented) A variety of 3,5-disubstituted 4-halo(seleno)isoxazoles are readily prepared in good to excellent yields under mild reaction conditions by the reaction of 2-alkyn-1-one O-methyl oximes with ICI, I2, Br2,
