2647-29-2Relevant articles and documents
Coupling Radical Homoallylic Expansions with C-C Fragmentations for the Synthesis of Heteroaromatics: Quinolines from Reactions of o-Alkenylarylisonitriles with Aryl, Alkyl, and Perfluoroalkyl Radicals
Evoniuk, Christopher J.,Gomes, Gabriel Dos Passos,Ly, Michelle,White, Frankie D.,Alabugin, Igor V.
, p. 4265 - 4278 (2017/04/27)
Selective addition of radicals to isonitriles can be harnessed for initiating reaction cascades designed to overcome the stereoelectronic restrictions on homoallylic ring expansion in alkyne reactions and to develop a new general route for the preparation of N-heteroaromatics. This method utilizes alkenes as synthetic equivalents of alkynes by coupling homoallylic ring expansion to yield the formal "6-endo" products with aromatization via stereoelectronically assisted C-C bond scission. Computational analysis of the homoallyic expansion potential energy surface reveals that the indirect 5-exo/3-exo/retro-3-exo path is faster than the direct 6-endo-trig closure, revealing the general exo-preference for the cyclization processes.
Synthetic utility of propylphosphonic anhydridedmso media: An efficient one-pot three-component synthesis of 2-arylquinolines
Narasimhamurthy, Kereyagalahally H.,Chandrappa, Siddappa,Kumar, Kothanahally S. Sharath,Swaroop, Toreshettahally R.,Rangappa, Kanchugarakoppal S.
supporting information, p. 1073 - 1075 (2013/09/24)
Propylphosphonic anhydride (T3P?)DMSO-mediated onepot three-component synthesis which provides 2-arylquinolines in a single step from benzyl alcohols, anilines, and ethyl vinyl ether by the modified Povarov reaction has been demonstrated. T3P?DMSO is a mild and low-toxic peptide coupling agent and an easy to handle reagent for bulk reactions at room temperature.
